Clinical Trial

RIPB Versus EOIPB for Pain Control After Laparoscopic Cholecystectomy

Study acronym: RIPB-EOIPB
Recruiting
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Summary
This prospective observational study aims to compare the effects of bilateral ultrasound-guided recto-intercostal plane block(RIPB) and bilateral ultrasound-guided external oblique intercostal plane block(EOIPB) on postoperative analgesia in patients undergoing elective laparoscopic cholecystectomy under general anesthesia. Both blocks are performed after anesthesia induction as part of routine preemptive multimodal analgesia practice. Patients who receive bilateral recto-intercostal plane block will be included in the RIPB group, and patients who receive bilateral external oblique intercostal plane block will be included in the EOIPB group. The primary outcome is cumulative intravenous tramadol consumption via patient-controlled analgesia during the first 24 postoperative hours. Secondary outcomes include postoperative pain scores at rest and during activity, rescue analgesic requirement, postoperative nausea and vomiting, time to mobilization, length of hospital stay, quality of recovery assessed using the Quality of Recovery-15 questionnaire, and block-related complications.
Protocol Amendment History 3 changes
critical Trial completed 2026-06-12
notable Primary completion moved earlier: 2026-07-22 -> 2026-06-09 2026-06-12
minor Completion moved earlier: 2026-10-25 -> 2026-06-09 2026-06-12
Trial Details
NCT Number NCT07607262
Lead Sponsor Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital
Conditions Laparoscopic Cholecystectomy, Postoperative Pain, Postoperative Analgesia
Enrollment 60 participants
Start Date 2026-05-15
Primary Completion 2026-06-09 (estimated)
Study Completion 2026-10-09 (estimated)
Updated on ClinicalTrials.gov 2026-07-10