Bupivacaine irrigation for pain after gallbladder surgery
Official title: Comparison of Intraperitoneal Bupivacaine and Normal Saline Irrigation for Postoperative Pain Relief After Laparoscopic Cholecystectomy
Run by Wah Medical college , POF hospital · NCT07650760 · Data updated 2026-11-12
This trial tests whether irrigating the abdominal cavity with bupivacaine reduces pain after laparoscopic cholecystectomy compared with saline irrigation in adults 18–60.
Quick facts
| Phase | Phase 4 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years to 60 Years |
| Sex | All |
| Enrollment | 106 (estimated) |
| Sponsor | Wah Medical college , POF hospital Academic / other |
| Locations | 1 site (Wāh, Punjab Province) |
| Status | Recruiting |
| Started | July 1, 2026 |
| Main results expected | December 2026 |
| Study ends | December 2026 |
| Registry record updated | June 16, 2026 |
| Trial ID | NCT07650760 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18–60 undergoing elective laparoscopic cholecystectomy without choledocholithiasis, pancreatitis, or contraindications to bupivacaine or saline.
✕Probably not a fit
Patients with contraindications to bupivacaine, those converting to open surgery, or those unable to report pain may not benefit from this approach.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized, double-blind trial compares intraperitoneal irrigation with bupivacaine to saline after elective laparoscopic cholecystectomy. A total of 106 adults are evenly assigned to each group, with standardized surgical procedures aside from the irrigation solution. The primary outcome is postoperative pain measured by a visual analog scale, with follow-up during recovery and early postoperative period. Blinding is maintained for both surgeons and patients to avoid bias. Eligibility excludes those with biliary complications, pregnancy, inability to report pain, or contraindications to the study drugs.
Why it matters
Potential benefit: If successful, this approach could provide better pain control and reduce reliance on systemic analgesics after gallbladder surgery.
How similar studies have gone: Previous studies suggested bupivacaine can reduce postoperative pain, but results vary and more evidence is needed for routine adoption.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * • Adult consented patients of any gender aged 18 to 60 years Fit to undergo elective laparoscopic cholecystectomy Exclusion Criteria: * • Patients who had developed choledocholithiasis or pancreatitis pre-operatively * Where conversion to open cholecystectomy is needed intraoperatively * Pregnant or lactating * Inability to express pain appropriately, like in psychiatric disorders * With any contraindication to the use of bupivacaine or normal saline, e.g., hypersensitivity
Where it's running
-
Wah Medical College, POF Hospital Wah cantt Wāh
Wāh, Punjab Province, Pakistan Recruiting
Study contacts
- Study coordinator: Muhammad Asad Janjua, MBBS
- Email: asad24871@gmail.com
- Phone: 00923351589093
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.