Clinical trial Recruiting at 1 site Interventional Ages 18 to 80

Rectointercostal plane block to reduce pain after laparoscopic gallbladder removal

Official title: Evaluation of the Effect of Ultrasound-Guided Bilateral Recto-Intercostal Fascial Plane Block on Postoperative Pain, Opioid Consumption, and Quality of Recovery in Laparoscopic Cholecystectomy Surgery: A Prospective, Randomized, Double-Blind Controlled Clinical Study

Run by Istinye University · NCT07745972 · Data updated 2026-11-12

This study tests whether giving a rectointercostal block during laparoscopic cholecystectomy can lower postoperative pain for patients without changing general anesthesia.

Quick facts

Study typeInterventional
Ages18 Years to 80 Years
SexAll
Enrollment60 (estimated)
SponsorIstinye University
Academic / other
Locations1 site (Istanbul)
StatusRecruiting
StartedAugust 6, 2026
Main results expectedDecember 31, 2026
Study endsDecember 31, 2026
Registry record updatedAugust 10, 2026
Trial IDNCT07745972 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults with BMI under 35 kg/m² and ASA I–II undergoing laparoscopic cholecystectomy, without contraindications to regional anesthesia.

Probably not a fit

Patients with higher BMI, higher ASA status, bleeding disorders, or allergies to local anesthetics may not receive benefit and could be at higher risk.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

In this randomized trial, patients undergoing laparoscopic cholecystectomy are assigned to receive a rectointercostal fascial plane block with bupivacaine 0.25% or no regional block, in addition to standard general anesthesia. The blocking procedure is performed before extubation by an experienced anesthesiologist and is concealed from the patient; the block administrator and pain assessors are blinded to group assignment. Postoperative pain outcomes are collected by a separate blinded assessor to determine the block’s effectiveness in improving analgesia. Inclusion criteria include BMI less than 35 and ASA I–II, while several conditions exclude participation, such as coagulopathy or allergy to local anesthetics. The trial is conducted at Istinye University with randomization via computer-generated codes and independent allocation concealment.

Why it matters

Potential benefit: If successful, patients may experience less postoperative pain and reduced analgesic needs after laparoscopic cholecystectomy.

How similar studies have gone: Prior regional blocks have shown pain reduction in abdominal surgery, but this specific rectointercostal plane block approach for cholecystectomy is being evaluated in this setting.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* BMI \< 35 kg/m²
* Patients with ASA scores I and II

Exclusion Criteria:

* Patients who do not want to be included in the study
* Psychiatric and neurological disease with blurred consciousness
* Patients with ASA \> 3
* BMI \> 35 kg/m²
* Abnormality in coagulation parameters
* History of allergy to local anesthetic drugs
* Infection at the injection site

Where it's running

  • Istinye University Liv Topkapı Hospital
    Istanbul, Turkey (Türkiye)
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.