RecruitingNot ApplicableNCT06976320

Deep Rectus Sheath Block for Laparoscopic Cholecystectomy

Deep Rectus Sheath Block for Postoperative Analgesia in Patients Undergoing Laparoscopic Cholecystectomy


Sponsor

Istinye University

Enrollment

60 participants

Start Date

Sep 9, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Postoperative pain after laparoscopic cholecystectomy can be considerable. Regional techniques such as erector spinae plane (ESP) block or transversus abdominis plane (TAP) block may be suitable for patients at increased risk of postoperative pain. The deep rectus sheath block is a novel block which is a modified version of the conventional rectus sheath block. It was reported in a few case reports that, it may be used for postoperative analgesia in patients undergoing laparoscopic cholecystectomy. The aim of this study is to investigate the postoperative analgesic efficacy of deep rectus sheath block in patients undergoing laparoscopic cholecystectomy.


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Deep rectus sheath block, Intravenous morphine patient control analgesia, and others for people with anesthesia, cholecystectomy, laparoscopic, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 80 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERIntravenous morphine patient control analgesia

24-hour morphine consumption will be recorded

OTHERIntravenous patient control analgesia

24-hour morphine consumption will be recorded

OTHERDeep rectus sheath block

Deep rectus sheath block will be administered at the end of the surgery.


Locations(1)

Istinye University Hospital

Istanbul, Turkey (Türkiye)

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NCT06976320


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