Deep Rectus Sheath Block for Laparoscopic Cholecystectomy
Condition(s) studied
Investigational drug(s) / intervention(s)
Intravenous morphine patient control analgesia: 24-hour morphine consumption will be recorded
Intravenous patient control analgesia: 24-hour morphine consumption will be recorded
Deep rectus sheath block: Deep rectus sheath block will be administered at the end of the surgery.
Study 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
Primary outcome measure(s)
- Morphine consumption — Postoperative 24 hours
The amount of morphine required by the patient and given by the device will be recorded for the first 24 hours.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Istinye University Hospital | Istanbul | Turkey (Türkiye) | Recruiting |
More Istinye University trials in Turkey
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06976320 on ClinicalTrials.gov ↗ ← All trials in Turkey