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Comparing patient comfort and recovery after two minimally invasive gall bladder surgeries.

Comparative study on surgical outcomes in 3-port versus 4-port laparoscopic cholecystectomy: A randomized control trial in a tertiary care centre of eastern Uttar Pradesh - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/106188
Enrollment
80
Registered
2026-03-13
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K802- Calculus of gallbladder without cholecystitis Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: 3 port: Participants randomized to the intervention arm will undergo three-port laparoscopic cholecystectomy. After induction of general anesthesia and creation of pneumoperitoneum usin

Sponsors

Dr Pearl Yadav
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Symptomatic gallstone disease planned for elective surgery

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
1.Postoperative Pain 2.Operative time 3.Intraoperative and Postoperative ComplicationsTimepoint: Pain intensity will be measured using the Visual Analogue Scale (VAS) at predefined intervals (6, 12, and 24 hours). Total duration of surgery will be measured from skin incision to skin closure, and time taken from skin incision to complete dissection of Calot s triangle. Documentation of complications, including bile duct injury, haemorrhage, and other adverse events will be done.

Secondary

MeasureTime frame
Conversion RateTimepoint: Incidence of conversion from three-port to four-port laparoscopic cholecystectomy or to open surgery, along with underlying indications will be noted.;Postoperative Analgesic RequirementTimepoint: Quantification of analgesic consumption (type, dose, and frequency) in addition to prescribed analgesics will be done.;Return to Normal ActivitiesTimepoint: Time taken to resume daily activities will be recorded in days.;Length of Hospital StayTimepoint: Total postoperative hospital stay will be measured in days;Patient SatisfactionTimepoint: Assessment of cosmetic outcomes will be done using validated scoring tools at the time of suture removal;Surgeon Ergonomics and ComfortTimepoint: Evaluation of ergonomic strain, posture, and physical discomfort using standardized ergonomic assessment tools

Countries

India

Contacts

Public ContactDr Mukul Singh

All India Institute of Medical Sciences Gorakhpur

singhmukul3911@gmail.com9997343119

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Apr 4, 2026