Skip to content
MDThesis

MS · General Surgery

General Surgery thesis topics, with the design and feasibility for each


Almost every general surgery thesis is built out of the emergency theatre register and the elective operating list, which means your sample accrues at the speed your unit actually operates. The commonest failure is a design that needs follow-up at six months in a population that does not return after suture removal, so decide early whether your primary outcome is measured before discharge or needs a clinic visit. Examiners press hardest on how the comparison arms were allocated, on who assessed the outcome, and on whether wound outcomes were scored against a stated definition rather than the operating surgeon's impression.

Topic register · 46 entries · 8 designs[6]

  • NMC PGMER-2023
  • NBEMS 180 days / 26 months
  • UGC 2018 · under 10%
  • ICMR 2017 · ethics

The register

Filter, read, copy

The General Surgery register

Authored by the practice · Not compiled from any list


Filter by design or by feasibility, or search the titles and outcomes. Filtering only hides entries: every topic stays on the page, so nothing is lost if you clear the filters or arrive by a deep link.

Feasibility in a teaching unit

Showing 46 of 46 topics

The sample figure on each plate is a planning range read off the design, not a calculated answer. Your own number comes from a calculation against your own assumptions — the difference you would call clinically meaningful, the variability in your setting, the power you want — and it belongs in the synopsis with those assumptions written beside it.

  • Topic 01 / 46

    Link to this entry

    Comparison of the Alvarado and RIPASA scores against histopathology in patients operated for suspected acute appendicitis

    DesignDiagnostic accuracyFeasibilityStraightforward
    Primary outcome
    Sensitivity, specificity and predictive values of each score against the histopathological diagnosis of appendicitis
    Collection time
    10–12 months of consecutive emergency admissions
    Sample, as a planning figure
    roughly 130–180 suspected cases, governed by the expected sensitivity and the proportion found to have appendicitis, subject to a proper calculation

    What your unit must already have

    • a steady emergency surgical intake of suspected appendicitis
    • histopathology reporting of every appendicectomy specimen
    • a scoring proforma completed before the decision to operate

    What derails it

    Both scores must be recorded before the surgeon decides to operate; if the resident fills the proforma after the theatre list is made, the score has been contaminated by the decision it is meant to predict and the whole dataset is unusable.

  • Topic 02 / 46

    Link to this entry

    Adult Appendicitis Score as a triage tool for admission and observation in right iliac fossa pain

    DesignDiagnostic accuracyFeasibilityStraightforward
    Primary outcome
    Proportion correctly assigned to low, intermediate and high probability groups, judged against final diagnosis at discharge
    Collection time
    9–12 months
    Sample, as a planning figure
    roughly 150–200 consecutive patients presenting with right iliac fossa pain, subject to a proper calculation

    What your unit must already have

    • emergency department access to patients before surgical referral
    • total leucocyte count and CRP available round the clock
    • a follow-up mechanism for patients discharged without operation

    What derails it

    The score needs CRP, and in many units CRP is sent only when the consultant asks for it, so a quarter of your proformas end up with that single field blank and have to be excluded.

  • Topic 03 / 46

    Link to this entry

    Histologically negative appendicectomy in a teaching unit: frequency and associated clinical features

    DesignRetrospectiveFeasibilityStraightforward
    Primary outcome
    Proportion of appendicectomy specimens reported as normal, and the clinical and laboratory features associated with them
    Collection time
    3–4 months of record retrieval for a three-year period
    Sample, as a planning figure
    roughly 300–500 archived appendicectomies, limited by what the period contains rather than by calculation

    What your unit must already have

    • theatre and histopathology registers covering at least three years
    • case sheets retrievable by operation code
    • an ethics committee waiver of consent for record review

    What derails it

    Histopathology reports from different pathologists describe normal appendices in different language, so agree a single written definition of a negative specimen with the pathology department before abstraction or your numerator keeps moving.

  • Topic 04 / 46

    Link to this entry

    Antibiotic-first management compared with early appendicectomy in radiologically uncomplicated acute appendicitis

    DesignComparative interventionalFeasibilityModerate
    Primary outcome
    Treatment success at one month, defined as resolution without appendicectomy in the antibiotic arm
    Collection time
    12–15 months of enrolment with one month of follow-up
    Sample, as a planning figure
    roughly 50–70 per arm, subject to a proper calculation

    What your unit must already have

    • ultrasound or CT to exclude perforation and appendicolith before allocation
    • consultant agreement that non-operative management is offered in the unit
    • a telephone follow-up system for the first month

    What derails it

    Consent is the bottleneck — patients who have been told they have appendicitis usually want it removed, and if the surgeon on call also prefers to operate, recruitment into the antibiotic arm stalls at a handful of patients.

  • Topic 05 / 46

    Link to this entry

    Outcome of conservative management of appendicular lump with planned interval appendicectomy

    DesignProspective observationalFeasibilityStraightforward
    Primary outcome
    Proportion resolving on conservative management without emergency surgery, and complications at interval appendicectomy
    Collection time
    12–15 months
    Sample, as a planning figure
    roughly 40–60 patients, depending on how often lumps present in your unit, subject to a proper calculation

    What your unit must already have

    • serial clinical and ultrasound assessment of the lump
    • inpatient beds for an initial period of observation
    • an elective list that can accommodate interval cases at six to eight weeks

    What derails it

    A third of patients feel well after discharge and never come back for the interval appendicectomy, so your outcome at eight weeks must be defined so that a non-attender is still classified rather than lost.

  • Topic 06 / 46

    Link to this entry

    Laparoscopic compared with open appendicectomy in acute appendicitis: postoperative pain, wound complications and hospital stay

    DesignComparative interventionalFeasibilityModerate
    Primary outcome
    Visual analogue pain score at 24 hours and length of postoperative hospital stay
    Collection time
    12 months
    Sample, as a planning figure
    roughly 45–65 per arm, subject to a proper calculation

    What your unit must already have

    • a functioning laparoscopic set available for emergency lists
    • surgeons who do emergency laparoscopy routinely, not occasionally
    • a standard analgesia protocol applied to both arms

    What derails it

    Laparoscopy in most units happens on the day a particular consultant is on call, so allocation follows the duty roster and the arms differ in who operated as much as in how — state this openly and match for operator grade or the comparison will be attacked.

  • Topic 07 / 46

    Link to this entry

    Lichtenstein mesh hernioplasty compared with Desarda no-mesh repair in primary inguinal hernia

    DesignRandomised controlledFeasibilityModerate
    Primary outcome
    Pain on a visual analogue scale at one month and time to return to routine activity
    Collection time
    12–15 months of enrolment with three months of follow-up
    Sample, as a planning figure
    roughly 40–60 per arm, subject to a proper calculation

    What your unit must already have

    • an elective hernia list with reliable weekly numbers
    • surgeons trained in the Desarda technique
    • CTRI registration before the first patient is enrolled

    What derails it

    Return to routine activity means something different to a farmer and to a bank clerk, so define it as a written milestone at enrolment and record occupation, otherwise the difference you measure is occupational rather than surgical.

  • Topic 08 / 46

    Link to this entry

    Totally extraperitoneal compared with transabdominal preperitoneal repair in inguinal hernia: operative time and early complications

    DesignComparative interventionalFeasibilityDemanding
    Primary outcome
    Operative time and the rate of seroma, port-site complications and conversion within one month
    Collection time
    15–18 months
    Sample, as a planning figure
    roughly 30–45 per arm, subject to a proper calculation

    What your unit must already have

    • a unit doing laparoscopic hernia repair as routine practice
    • at least two surgeons comfortable with both approaches
    • theatre records that capture operative time accurately

    What derails it

    Most units favour one of the two approaches, so the second arm fills at a trickle; confirm from last year's theatre register that both were done at least twice a month before committing to this.

  • Topic 09 / 46

    Link to this entry

    Chronic groin pain six months after open mesh hernioplasty and its preoperative predictors

    DesignCohortFeasibilityStraightforward
    Primary outcome
    Presence of groin pain at six months graded on a visual analogue scale
    Collection time
    12 months of enrolment with six months of follow-up
    Sample, as a planning figure
    roughly 90–130 patients allowing for attrition, subject to a proper calculation

    What your unit must already have

    • an elective hernia list with consistent numbers
    • a documented preoperative pain and sensation assessment
    • a follow-up clinic with telephone recall at six months

    What derails it

    Six-month follow-up is where this study dies; patients who are comfortable are the least likely to attend, which loads your sample with the symptomatic and inflates the very outcome you are measuring.

  • Topic 10 / 46

    Link to this entry

    Onlay compared with sublay mesh placement in elective incisional hernia repair

    DesignComparative interventionalFeasibilityModerate
    Primary outcome
    Seroma formation and surgical site occurrence within 30 days
    Collection time
    15 months
    Sample, as a planning figure
    roughly 35–50 per arm, subject to a proper calculation

    What your unit must already have

    • a regular load of elective incisional hernia cases
    • suction drain management recorded on a standard chart
    • ultrasound access for confirming clinically suspected seroma

    What derails it

    Seroma is diagnosed inconsistently unless you define it by a stated volume on ultrasound at a fixed postoperative day; counting only seromas that needed aspiration measures the surgeon's aspiration habit, not the repair.

  • Topic 11 / 46

    Link to this entry

    Factors associated with incisional hernia after emergency midline laparotomy: a case-control comparison

    DesignCase-controlFeasibilityStraightforward
    Primary outcome
    Association of wound infection, body mass index, anaemia and closure technique with the presence of incisional hernia
    Collection time
    6–8 months of record review and clinic recall
    Sample, as a planning figure
    roughly 50–70 cases with one or two controls each, subject to a proper calculation

    What your unit must already have

    • a traceable register of emergency laparotomies from two to four years earlier
    • operative notes that record the closure material and technique
    • an ethics waiver for record review plus consent for examining recalled patients

    What derails it

    Controls must come from the same laparotomy cohort and be examined for an occult hernia, because picking controls from people who simply never returned guarantees you have misclassified some of them as hernia-free.

  • Topic 12 / 46

    Link to this entry

    Cyanoacrylate glue compared with polypropylene suture for mesh fixation in Lichtenstein hernioplasty

    DesignRandomised controlledFeasibilityModerate
    Primary outcome
    Early postoperative pain on a visual analogue scale at 48 hours and at one month
    Collection time
    12–15 months
    Sample, as a planning figure
    roughly 35–50 per arm, subject to a proper calculation

    What your unit must already have

    • a reliable supply of surgical glue for the whole study period
    • an assessor recording pain who did not operate
    • CTRI registration before enrolment

    What derails it

    Glue is bought in small quantities and runs out mid-study in most units, and a two-month gap in supply leaves you with arms recruited in different seasons and different residents operating — secure the full quantity in writing first.

  • Topic 13 / 46

    Link to this entry

    Negative pressure wound therapy compared with conventional moist dressing in diabetic foot ulcers

    DesignRandomised controlledFeasibilityModerate
    Primary outcome
    Percentage reduction in wound surface area at four weeks measured by planimetry on standardised photographs
    Collection time
    12–15 months
    Sample, as a planning figure
    roughly 30–45 per arm, subject to a proper calculation

    What your unit must already have

    • working negative pressure units and consumables for the full period
    • a fixed photographic protocol with a scale marker for wound measurement
    • glycaemic control and offloading standardised across both arms

    What derails it

    Consumable cost decides who gets the therapy in real life, so if the patient pays for the canister your allocation quietly becomes economic rather than random — budget the consumables into the protocol or the randomisation collapses.

  • Topic 14 / 46

    Link to this entry

    Wagner grade at presentation and subsequent minor or major amputation in diabetic foot ulcer

    DesignProspective observationalFeasibilityStraightforward
    Primary outcome
    Amputation at any level within three months of presentation
    Collection time
    12 months of enrolment with three months of follow-up
    Sample, as a planning figure
    roughly 100–140 patients, subject to a proper calculation

    What your unit must already have

    • a diabetic foot clinic or surgical OPD with consistent referrals
    • ankle-brachial index measurement or Doppler access
    • a record system that captures amputations done elsewhere on readmission

    What derails it

    Patients who go home and have a toe amputated at a nursing home count as events but never appear in your register, so build a telephone check at three months into the proforma rather than relying on your own theatre records.

  • Topic 15 / 46

    Link to this entry

    Honey dressing compared with povidone-iodine dressing in chronic non-healing lower limb ulcers

    DesignComparative interventionalFeasibilityStraightforward
    Primary outcome
    Proportion of ulcer floor covered by healthy granulation tissue at three weeks
    Collection time
    10–12 months
    Sample, as a planning figure
    roughly 30–45 per arm, subject to a proper calculation

    What your unit must already have

    • a dressing room with consistent daily dressing practice
    • medical grade honey of a single stated source throughout
    • photographic documentation at fixed intervals

    What derails it

    Granulation assessed by the resident doing the dressing is the soft spot here; have a second observer grade the photographs blind to the dressing, because the honey is visible on the wound and cannot be masked at the bedside.

  • Topic 16 / 46

    Link to this entry

    Surgical site infection after elective abdominal surgery: rate, organisms and sensitivity pattern

    DesignProspective observationalFeasibilityStraightforward
    Primary outcome
    Surgical site infection within 30 days, classified by CDC criteria, with the organism isolated
    Collection time
    12 months of enrolment with 30 day follow-up
    Sample, as a planning figure
    roughly 200–300 consecutive elective procedures, subject to a proper calculation

    What your unit must already have

    • microbiology support for wound swab culture and sensitivity
    • agreement to apply CDC wound classification at every dressing
    • a 30 day telephone or clinic follow-up for discharged patients

    What derails it

    Many infections declare themselves only after discharge, towards the end of the first week and into the second, so a study that stops counting at discharge reports a figure about bed occupancy rather than about infection.

  • Topic 17 / 46

    Link to this entry

    Skin staples compared with subcuticular monofilament suture for closure of clean elective abdominal incisions

    DesignRandomised controlledFeasibilityStraightforward
    Primary outcome
    Surgical site infection at 30 days and patient-reported scar satisfaction at three months
    Collection time
    12 months
    Sample, as a planning figure
    roughly 50–70 per arm, subject to a proper calculation

    What your unit must already have

    • a steady elective clean-case list
    • staplers stocked for the full study period
    • a blinded observer for wound and scar assessment

    What derails it

    Wound assessment cannot be blinded while the staples are in place, so schedule the scar assessment after removal and use photographs graded by someone outside the operating team.

  • Topic 18 / 46

    Link to this entry

    Nutritional status by Subjective Global Assessment in patients awaiting major elective gastrointestinal surgery

    DesignCross-sectionalFeasibilityStraightforward
    Primary outcome
    Distribution of Subjective Global Assessment categories, with anthropometry and serum albumin
    Collection time
    8–10 months
    Sample, as a planning figure
    roughly 200–280 patients attending for preoperative assessment, subject to a proper calculation

    What your unit must already have

    • a preoperative assessment clinic where patients can be interviewed unhurried
    • weighing scale, stadiometer and mid-arm circumference tape
    • serum albumin as part of routine preoperative work-up

    What derails it

    Subjective Global Assessment depends on a reported weight loss over six months, and patients who have never owned a weighing scale cannot give it, so decide in advance how you will handle that field rather than guessing from the clothes.

  • Topic 19 / 46

    Link to this entry

    Bethesda-categorised fine needle aspiration cytology against final histopathology in solitary thyroid nodule

    DesignDiagnostic accuracyFeasibilityStraightforward
    Primary outcome
    Sensitivity, specificity and rate of malignancy by Bethesda category against the resected specimen
    Collection time
    12–15 months
    Sample, as a planning figure
    roughly 80–120 operated nodules, governed by the expected proportion malignant, subject to a proper calculation

    What your unit must already have

    • cytology reported in Bethesda categories by the pathology department
    • a thyroid surgery list with consistent weekly numbers
    • ultrasound reporting that records nodule size and character

    What derails it

    Only operated nodules have a histological reference standard, so the benign categories are systematically under-represented; say so in your limitations and do not present the figures as if every aspirate had been verified.

  • Topic 20 / 46

    Link to this entry

    Voice outcome after total thyroidectomy assessed by the Voice Handicap Index-10 and laryngoscopy

    DesignProspective observationalFeasibilityModerate
    Primary outcome
    Change in Voice Handicap Index-10 score from before surgery to three months after
    Collection time
    15 months of enrolment with three months of follow-up
    Sample, as a planning figure
    roughly 50–70 patients, subject to a proper calculation

    What your unit must already have

    • preoperative and postoperative flexible laryngoscopy, usually via the ENT department
    • a translated and pretested Voice Handicap Index-10 in the local language
    • a thyroidectomy volume of at least three or four a month

    What derails it

    The instrument must be administered in the patient's own language and the same version every time; a resident translating the ten items afresh at each visit destroys comparability between the preoperative and postoperative scores.

  • Topic 21 / 46

    Link to this entry

    Early postoperative parathyroid hormone and serum calcium as predictors of symptomatic hypocalcaemia after total thyroidectomy

    DesignProspective observationalFeasibilityModerate
    Primary outcome
    Symptomatic hypocalcaemia within 72 hours requiring calcium supplementation
    Collection time
    15–18 months
    Sample, as a planning figure
    roughly 60–90 patients, subject to a proper calculation

    What your unit must already have

    • parathyroid hormone assay available with a turnaround usable in hours
    • serial serum calcium at fixed postoperative time points
    • enough total thyroidectomies rather than mainly hemithyroidectomies

    What derails it

    The parathyroid hormone sample has to be drawn at a fixed hour after surgery, and on a busy evening list that sample is the one that gets missed — name the time point in the proforma and brief the night resident.

  • Topic 22 / 46

    Link to this entry

    Drain compared with no drain after hemithyroidectomy for benign thyroid nodule

    DesignRandomised controlledFeasibilityStraightforward
    Primary outcome
    Postoperative neck collection on ultrasound at 48 hours and length of hospital stay
    Collection time
    15 months
    Sample, as a planning figure
    roughly 30–45 per arm, subject to a proper calculation

    What your unit must already have

    • a thyroid list with a predominance of benign hemithyroidectomies
    • bedside or radiology ultrasound at 48 hours
    • CTRI registration before enrolment

    What derails it

    Surgeons place a drain out of habit and will break allocation for a case that bled a little more than usual, so record every protocol deviation as it happens rather than discovering a contaminated no-drain arm at analysis.

  • Topic 23 / 46

    Link to this entry

    Triple assessment of the palpable breast lump against histopathology of the excised specimen

    DesignDiagnostic accuracyFeasibilityStraightforward
    Primary outcome
    Sensitivity and specificity of combined clinical examination, ultrasound and cytology against histopathology
    Collection time
    12 months
    Sample, as a planning figure
    roughly 100–150 palpable lumps proceeding to histology, subject to a proper calculation

    What your unit must already have

    • ultrasound reporting with a stated BIRADS category
    • cytology or core biopsy on the same visit
    • histopathology on every excised or biopsied lump

    What derails it

    Young women with a clinically obvious fibroadenoma are often not excised, so if you include only operated lumps your specificity is measured in a population that has already been filtered by the surgeon's suspicion.

  • Topic 24 / 46

    Link to this entry

    Flap fixation compared with conventional closure after modified radical mastectomy: seroma formation and drain duration

    DesignComparative interventionalFeasibilityModerate
    Primary outcome
    Total drain output and number of post-drain-removal seroma aspirations within four weeks
    Collection time
    15–18 months
    Sample, as a planning figure
    roughly 30–45 per arm, subject to a proper calculation

    What your unit must already have

    • a breast cancer operative load of at least three mastectomies a month
    • a standard drain removal criterion stated in millilitres per day
    • a nursing chart that records daily drain volume reliably

    What derails it

    Daily drain volume is the primary data and it is recorded by whichever nurse is on duty; if the chart is filled once a shift by estimate, your main variable has been eyeballed and the comparison means nothing.

  • Topic 25 / 46

    Link to this entry

    Shoulder morbidity after axillary lymph node dissection assessed by the QuickDASH and goniometry

    DesignProspective observationalFeasibilityModerate
    Primary outcome
    QuickDASH score and shoulder abduction range at three months compared with the preoperative value
    Collection time
    15 months of enrolment with three months of follow-up
    Sample, as a planning figure
    roughly 45–65 patients, subject to a proper calculation

    What your unit must already have

    • a goniometer and a single trained observer for all measurements
    • a translated QuickDASH administered consistently
    • physiotherapy advice standardised for every patient

    What derails it

    Patients start adjuvant chemotherapy between your baseline and three-month visits and their attendance follows the chemotherapy calendar, so align your assessment with an existing oncology visit or half the cohort will be measured weeks late.

  • Topic 26 / 46

    Link to this entry

    Clinicopathological profile of breast carcinoma in women under forty treated at a teaching hospital

    DesignRetrospectiveFeasibilityStraightforward
    Primary outcome
    Distribution of stage, grade and hormone receptor status at presentation
    Collection time
    4–5 months of record retrieval over a five-year period
    Sample, as a planning figure
    roughly 100–200 archived cases, limited by what the period contains

    What your unit must already have

    • a tumour register or histopathology archive spanning five years
    • immunohistochemistry reports available for most cases
    • an ethics waiver of consent for record review

    What derails it

    Receptor status is missing in a substantial share of older files because the test was done outside and the report never came back to the chart, so decide how missing immunohistochemistry will be handled before you start abstraction.

  • Topic 27 / 46

    Link to this entry

    Preoperative clinical and ultrasound predictors of conversion from laparoscopic to open cholecystectomy

    DesignProspective observationalFeasibilityStraightforward
    Primary outcome
    Conversion to open surgery during the index procedure
    Collection time
    12 months
    Sample, as a planning figure
    roughly 150–220 consecutive laparoscopic cholecystectomies, subject to a proper calculation

    What your unit must already have

    • a laparoscopic cholecystectomy volume of at least fifteen a month
    • ultrasound reports that state gall bladder wall thickness and pericholecystic collection
    • theatre records that document the reason for conversion

    What derails it

    Conversion depends heavily on who is operating, and a unit where the senior consultant converts almost never and a first-year resident converts often will produce a model that is really predicting the surgeon — record operator grade as a variable.

  • Topic 28 / 46

    Link to this entry

    Intraoperative difficulty grading at laparoscopic cholecystectomy and its relation to postoperative course

    DesignProspective observationalFeasibilityStraightforward
    Primary outcome
    Operative time, bile spillage and length of stay by intraoperative difficulty grade
    Collection time
    10–12 months
    Sample, as a planning figure
    roughly 120–180 procedures, subject to a proper calculation

    What your unit must already have

    • a single agreed difficulty grading scale displayed in theatre
    • the operating surgeon willing to record the grade at the end of each case
    • accurate operative start and finish times

    What derails it

    The grade must be assigned at the end of the operation and not reconstructed next morning from the notes, because by then the surgeon grades the case by how the patient is doing rather than by what the gall bladder looked like.

  • Topic 29 / 46

    Link to this entry

    Early compared with delayed laparoscopic cholecystectomy in acute calculous cholecystitis

    DesignComparative interventionalFeasibilityModerate
    Primary outcome
    Total hospital stay across both admissions, conversion rate and bile duct injury
    Collection time
    15 months
    Sample, as a planning figure
    roughly 35–50 per arm, subject to a proper calculation

    What your unit must already have

    • emergency theatre access within 72 hours of admission
    • consultant agreement that early surgery is offered in the unit
    • a system to capture the second admission in the delayed arm

    What derails it

    Patients in the delayed arm return with another attack or go elsewhere for surgery, and if you count only those who come back for elective surgery you have quietly removed the failures from the comparison.

  • Topic 30 / 46

    Link to this entry

    Incidentally reported gall bladder carcinoma in routine cholecystectomy specimens and its presenting features

    DesignRetrospectiveFeasibilityStraightforward
    Primary outcome
    Frequency of malignancy on histopathology among specimens sent as benign disease, with the clinical and operative features noted
    Collection time
    3–4 months of record review across three to five years
    Sample, as a planning figure
    roughly 800–1500 archived cholecystectomy reports, limited by what the archive holds

    What your unit must already have

    • a histopathology archive with searchable specimen type
    • linked operative notes and ultrasound reports
    • an ethics waiver for record review

    What derails it

    Some units do not send every gall bladder for histology, and that selection is the whole study — establish what proportion of cholecystectomies in your period actually had a specimen reported before you frame the question.

  • Topic 31 / 46

    Link to this entry

    Mannheim Peritonitis Index and Boey score as predictors of mortality in perforated peptic ulcer

    DesignProspective observationalFeasibilityStraightforward
    Primary outcome
    In-hospital mortality, compared between score strata
    Collection time
    12–15 months
    Sample, as a planning figure
    roughly 80–120 consecutive patients, subject to a proper calculation

    What your unit must already have

    • a regular emergency load of peptic perforation
    • admission vitals, creatinine and albumin recorded before surgery
    • a proforma completed at admission rather than after the outcome

    What derails it

    The Mannheim index needs the duration of symptoms, which patients report vaguely — fix a rule for converting 'two or three days' into hours before collection begins, and record the interval from onset to surgery as a variable in its own right.

  • Topic 32 / 46

    Link to this entry

    Aetiological spectrum and operative outcome of hollow viscus perforation peritonitis

    DesignProspective observationalFeasibilityStraightforward
    Primary outcome
    Site of perforation at laparotomy and 30 day morbidity and mortality
    Collection time
    12 months
    Sample, as a planning figure
    roughly 100–150 consecutive laparotomies for perforation, subject to a proper calculation

    What your unit must already have

    • emergency laparotomy volume sufficient for the target
    • histopathology of resected bowel margins where taken
    • a 30 day outcome check including readmission

    What derails it

    Typhoid and tuberculous perforation cannot be separated on operative appearance alone, so if you plan to report aetiology you must commit in advance to sending tissue for histology on every small bowel perforation.

  • Topic 33 / 46

    Link to this entry

    BISAP score at admission and severity of acute pancreatitis by revised Atlanta criteria

    DesignProspective observationalFeasibilityStraightforward
    Primary outcome
    Development of moderately severe or severe pancreatitis by the revised Atlanta classification
    Collection time
    12–15 months
    Sample, as a planning figure
    roughly 90–130 patients, subject to a proper calculation

    What your unit must already have

    • serum amylase or lipase and contrast CT available when indicated
    • an admission proforma including mental status and pleural effusion on chest radiograph
    • follow-through of transfers to medicine or the intensive care unit

    What derails it

    BISAP needs a chest radiograph within 24 hours for the pleural effusion item, and in many units the film is only taken when the patient deteriorates — that single missing item quietly makes your score non-calculable in the mildest cases.

  • Topic 34 / 46

    Link to this entry

    Causes and operative outcome of acute intestinal obstruction in adults

    DesignRetrospectiveFeasibilityStraightforward
    Primary outcome
    Distribution of causes at operation and in-hospital morbidity and mortality
    Collection time
    3–4 months of record review across three years
    Sample, as a planning figure
    roughly 200–350 archived admissions, limited by what the period contains

    What your unit must already have

    • admission and theatre registers for three years
    • operative notes that state the cause found
    • an ethics waiver for record review

    What derails it

    Patients managed conservatively and discharged are recorded under vague diagnoses and will be missed entirely if you search only the theatre register, which biases your cause distribution towards the operated.

  • Topic 35 / 46

    Link to this entry

    Focused assessment with sonography for trauma against contrast-enhanced CT in haemodynamically stable blunt abdominal trauma

    DesignDiagnostic accuracyFeasibilityModerate
    Primary outcome
    Sensitivity and specificity of sonography for free fluid and solid organ injury against CT as reference
    Collection time
    12–15 months
    Sample, as a planning figure
    roughly 120–180 patients, governed by the expected sensitivity and the proportion injured, subject to a proper calculation

    What your unit must already have

    • a trauma intake with CT available round the clock
    • residents trained and credentialled to perform the focused scan
    • the scan recorded before the CT report is seen

    What derails it

    The sonography must be done and written down before the CT, and in a busy casualty the patient is often wheeled straight to CT — agree a written pathway with the emergency department or your index test will be recorded after the reference standard.

  • Topic 36 / 46

    Link to this entry

    Revised Trauma Score at triage and in-hospital mortality in blunt trauma

    DesignProspective observationalFeasibilityStraightforward
    Primary outcome
    In-hospital mortality across Revised Trauma Score strata
    Collection time
    12 months
    Sample, as a planning figure
    roughly 250–400 trauma presentations, subject to a proper calculation

    What your unit must already have

    • a triage area where respiratory rate, systolic pressure and Glasgow Coma Scale are recorded on arrival
    • a register that follows the patient after admission or transfer
    • agreement with the emergency department on who records the score

    What derails it

    Respiratory rate is the field nobody measures in a crowded casualty, and it is one of three components — if it is counted by eye or copied as sixteen for everyone the score loses its discrimination entirely.

  • Topic 37 / 46

    Link to this entry

    Stapled haemorrhoidopexy compared with open haemorrhoidectomy in grade three haemorrhoids

    DesignComparative interventionalFeasibilityModerate
    Primary outcome
    Postoperative pain on a visual analogue scale over the first week and time to return to work
    Collection time
    15 months
    Sample, as a planning figure
    roughly 30–45 per arm, subject to a proper calculation

    What your unit must already have

    • stapler devices funded for the full study period
    • a proctology load of at least four operable cases a month
    • a pain diary the patient can complete at home

    What derails it

    The stapler is expensive and patients who can afford it self-select into that arm, so unless the device cost is covered by the study your two groups differ in income, occupation and how soon they need to be back at work.

  • Topic 38 / 46

    Link to this entry

    Magnetic resonance fistulography against operative findings in complex fistula-in-ano

    DesignDiagnostic accuracyFeasibilityModerate
    Primary outcome
    Agreement of MRI with operative findings on internal opening, tract course and secondary extensions
    Collection time
    15–18 months
    Sample, as a planning figure
    roughly 40–60 operated fistulas, subject to a proper calculation

    What your unit must already have

    • MRI access with a pelvic protocol and a radiologist willing to report to a fixed template
    • a surgical load of complex and recurrent fistulas
    • the operating surgeon recording findings before seeing the MRI report

    What derails it

    If the surgeon has read the MRI before operating, the operative 'reference standard' is contaminated by the test being evaluated — the operative proforma must be filled by someone who records findings first and reads the report afterwards.

  • Topic 39 / 46

    Link to this entry

    Topical diltiazem compared with lateral internal sphincterotomy in chronic anal fissure

    DesignRandomised controlledFeasibilityStraightforward
    Primary outcome
    Pain relief on a visual analogue scale and fissure healing at six weeks
    Collection time
    12 months
    Sample, as a planning figure
    roughly 35–50 per arm, subject to a proper calculation

    What your unit must already have

    • a steady OPD load of chronic fissure
    • compounded topical diltiazem available throughout
    • follow-up at two and six weeks with proctoscopic examination

    What derails it

    Adherence to a topical applied twice daily for six weeks is poor and unverifiable, so build in a tube-weighing or returned-tube check rather than asking the patient whether they used it.

  • Topic 40 / 46

    Link to this entry

    Limberg flap compared with primary midline closure for sacrococcygeal pilonidal sinus

    DesignComparative interventionalFeasibilityModerate
    Primary outcome
    Wound complication and recurrence within six months
    Collection time
    15–18 months of enrolment with six months of follow-up
    Sample, as a planning figure
    roughly 25–40 per arm, subject to a proper calculation

    What your unit must already have

    • surgeons comfortable with flap reconstruction
    • a pilonidal caseload of at least two or three a month
    • six-month follow-up with examination of the natal cleft

    What derails it

    Pilonidal sinus is not a common elective case in most units, so check last year's register for actual numbers; a study needing fifty per arm on a caseload of two a month cannot finish inside a postgraduate window.

  • Topic 41 / 46

    Link to this entry

    Venous Clinical Severity Score before and after surgery for primary varicose veins

    DesignProspective observationalFeasibilityStraightforward
    Primary outcome
    Change in Venous Clinical Severity Score at three months from the preoperative value
    Collection time
    12–15 months
    Sample, as a planning figure
    roughly 50–70 patients, subject to a proper calculation

    What your unit must already have

    • venous duplex ultrasound to confirm the pattern of reflux before surgery
    • a single observer scoring all patients
    • compression stockings available to every patient postoperatively

    What derails it

    The score includes an ulcer item and a compression item, and patients who stop wearing stockings because of the heat will shift that component independently of the surgery — record stocking use as a separate variable.

  • Topic 42 / 46

    Link to this entry

    Endovenous laser ablation compared with conventional stripping for great saphenous vein incompetence

    DesignComparative interventionalFeasibilityDemanding
    Primary outcome
    Occlusion of the treated segment on duplex ultrasound at three months and time to return to work
    Collection time
    18 months
    Sample, as a planning figure
    roughly 25–40 per arm, subject to a proper calculation

    What your unit must already have

    • an endovenous laser platform with consumables for the study period
    • duplex ultrasound follow-up by a consistent operator
    • a varicose vein caseload the unit can actually supply

    What derails it

    The laser fibre is a per-case consumable and units ration it to paying patients; unless the department funds it for the study the ablation arm fills only with those who can pay, which also determines how quickly they return to work.

  • Topic 43 / 46

    Link to this entry

    Outcome of acute thermal burns by total body surface area and inhalational involvement

    DesignProspective observationalFeasibilityModerate
    Primary outcome
    In-hospital mortality and length of stay by burn surface area band
    Collection time
    12–15 months
    Sample, as a planning figure
    roughly 100–150 admissions, depending on what the burns unit receives, subject to a proper calculation

    What your unit must already have

    • a designated burns ward with a consistent admission policy
    • surface area charted on a Lund and Browder diagram by a trained assessor
    • records that capture death after transfer or discharge against advice

    What derails it

    Surface area estimated in casualty by the rule of nines and later recharted on a Lund and Browder diagram can differ by enough to move patients between your bands — decide which assessment is the study variable and stick to it.

  • Topic 44 / 46

    Link to this entry

    An enhanced recovery protocol compared with conventional perioperative care in elective bowel surgery

    DesignComparative interventionalFeasibilityModerate
    Primary outcome
    Time to first passage of flatus and length of postoperative hospital stay
    Collection time
    15–18 months
    Sample, as a planning figure
    roughly 30–45 per arm, subject to a proper calculation

    What your unit must already have

    • anaesthesia department agreement on the analgesia and fluid components
    • nursing staff briefed on early mobilisation and early oral feeding
    • a defined discharge criterion applied to both arms

    What derails it

    Length of stay in a government hospital is decided as much by the patient's travel and the ward round day as by recovery, so use a written discharge-readiness criterion as well as the actual discharge date or the protocol will look ineffective.

  • Topic 45 / 46

    Link to this entry

    Gall stones detected on abdominal ultrasound performed for unrelated indications in adults

    DesignCross-sectionalFeasibilityStraightforward
    Primary outcome
    Proportion with gall stones on ultrasound, with age, sex and body mass index recorded
    Collection time
    6–9 months
    Sample, as a planning figure
    roughly 400–600 consecutive scans, subject to a proper calculation

    What your unit must already have

    • access to the radiology ultrasound log with indication recorded
    • radiologists willing to note gall bladder status on every scan
    • height and weight measured at the time of the scan

    What derails it

    People sent for an abdominal ultrasound are not the general population, so describe the source population exactly and resist writing this up as a community figure — the referral indication is the main bias and must be reported.

  • Topic 46 / 46

    Link to this entry

    Feasibility and outcome of day-care general surgical procedures in a teaching hospital

    DesignProspective observationalFeasibilityStraightforward
    Primary outcome
    Proportion discharged on the day of surgery without unplanned admission, and readmission within 48 hours
    Collection time
    12 months
    Sample, as a planning figure
    roughly 150–250 procedures, subject to a proper calculation

    What your unit must already have

    • a defined day-care list with anaesthesia support for early discharge
    • written discharge criteria and a telephone review at 48 hours
    • patients living within reachable distance of the hospital

    What derails it

    Unplanned overnight stay in most units happens because the patient has nowhere to go before the morning bus, not because of a surgical problem, so record the reason for every failed discharge in a closed list of categories.


The designs

What each design commits you to

The designs in this General Surgery register


The design is not a label on the title; it decides your ethics route, your timetable and the test that answers your primary question. Only the designs that appear above are explained here.

  • Cross-sectional

    2 topics

    One contact per participant. Usually the quickest to complete, and the design most often chosen when time is short.

  • Prospective observational

    15 topics

    Participants are followed after enrolment without allocating an intervention. Ethics approval must precede the first enrolment.

  • Retrospective

    4 topics

    Existing records only. Faster, but limited by what was recorded, and a waiver of consent is normally sought from the ethics committee.

  • Comparative interventional

    11 topics

    Two or more arms compared. Ethics scrutiny is heavier, and the protocol must state how allocation is handled.

  • Randomised controlled

    6 topics

    Allocation is randomised. Prospective interventional studies are registered with the Clinical Trials Registry of India before the first participant is enrolled.

  • Diagnostic accuracy

    6 topics

    An index test measured against a reference standard. The sample size depends on the expected sensitivity or specificity and the prevalence in your setting.

  • Case-control

    1 topic

    Cases and controls compared for prior exposure. Control selection is where these are most often criticised.

  • Cohort

    1 topic

    A defined group followed over time. Attrition is the usual threat, so plan for it in the sample size.

What the feasibility mark means

A judgement about a typical teaching unit, not about yours. Confirm the volume, the equipment and the co-operation a topic needs before your synopsis goes in, because after that the timetable stops being negotiable[2].

  • Straightforward

    27 topics

    Achievable in most teaching units with routine caseload and no equipment beyond what is already in use.

  • Moderate

    17 topics

    Achievable, but needs either a specific piece of equipment, a collaborating department, or a caseload you should confirm before committing.

  • Demanding

    2 topics

    Only take this on if your unit already has the volume, the equipment and the co-operation it needs. Confirm all three before your synopsis goes in.


Next steps

Before you commit to one

What to do with a topic you like


Three steps, in this order. None of them is us: the first is arithmetic, the second is your guide, the third is a search only you can run.

  1. Do the arithmetic

    The figure on each plate is a planning range, not an answer. Put your own assumptions — the difference you would call clinically meaningful, the variability you expect, the power you want — into the free sample size calculator, then divide the result by the eligible patients your unit sees in a month and see whether the months you have left permit it.

  2. Take it to your guide

    Nothing on this page is approved by anybody. Your guide and your department decide what is feasible in your unit, and your ethics committee decides whether it may start — before the first participant, not before the analysis[5]. Where your university ordinance is stricter than anything here, the ordinance wins[1].

  3. Run the search yourself

    We make no claim that any question here is novel, under-studied or a gap, because that depends on a literature search run today in your own field. Read what the search returns before you write the introduction, and be ready to say why the question is worth asking in your setting.

What a thesis in this field has to satisfy — the obligations, the statistics and the questions residents ask first — is set out on the General Surgery page. Other specialties are in the topic bank index, and the method is worked through in the guides.


Undertakings

Mechanisms, not promises

What protects your draft, and who owns the work


Each line below is a mechanism this platform implements or a published instrument it is built around. None of them is a guarantee, and we are affiliated with no regulator or university.

Protection of your work

  • Row-level security

    Every table enforces row-level access. You read your own record, and nothing else.

  • View-only streaming

    Drafts are streamed to you through an authenticated route, not handed over as a file.

  • Watermarked to you

    Every page you read carries your own name and email across it.

  • Download gated

    The final file unlocks when the fee is settled in full, and not before.

  • Mumbai region · DPDP 2023

    Your record and your documents are held in the Mumbai region, so India's Digital Personal Data Protection Act 2023 applies to them.

  • Anonymised data only

    We accept no patient identifiers. An NDA is available on request.

How this works

Instruments we work to

  • NMC PGMER-2023

    The thesis obligations set out in the postgraduate medical education regulations.

  • NBEMS

    DNB and DrNB protocol and thesis timelines, and the page limit, as published.

  • UGC 2018 · <10%

    The academic integrity convention we work to on every draft.

  • ICMJE · Vancouver

    Authorship criteria and reference style, applied as published.

  • No affiliation

    We work to these published instruments. We are affiliated to none of the bodies that issue them.

How this works

Authorship and the uniqueness check

  • Sole author

    Mentoring, editing, statistics and compliance. You remain the sole author of your thesis.

  • Not ghostwriting

    We will not write your thesis for you, and we will not be named in it.

  • MDSoftune

    Word-level uniqueness checking, built with REDENN Informatics Inc., Canada.

  • Every version

    Each draft is checked word by word before your university sees it.

How this works

MDThesis is an independent academic mentorship practice. It is not affiliated with, endorsed by, or acting for the NMC, NBEMS, UGC or any university.

Free feasibility call

Tell us where your thesis stands. A senior doctor will tell you what to do next.


A senior doctor replies within one working day. No obligation. MD, MS, DNB, DrNB, DM, MCh, MDS and international programmes.

Request for a feasibility call

No obligation


No spam. A senior mentor replies personally. Your details stay private.


Reply within one working day · No obligation · Your details are not shared

Prefer to write to us first? Contact the practice. We mentor and edit; you remain the sole author of your thesis.

Document: Topic bank — General Surgery · Revision 1 · Last reviewed

Issued by MDThesis, a brand of REDENN Informatics Private Limited