Clinical Trial

Effectiveness Of Modified-Thoracoabdominal Nerve Block Perichondrial Approach (M-TAPA) In Laparoscopic Cholecystectomy

Recruiting
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Record status
This record was last updated October 22, 2024 (before its estimated November 12, 2024 completion). Its status may not reflect the trial's current state.
Summary
The Goal of this clinical trial is to determine the advantages of using Peripheral Nerve Block by injecting drugs under the skin on both sides of the abdomen in the upper abdominal area in patients undergoing laparoscopic Cholecystectomy. Study participants will be divided into 2 groups, namely group P1 receiving Modified Thoracoabdominal Perichondrial Approach (M-TAPA) block anesthesia after laparoscopic cholecystectomy and group P2 only receiving intravenous opioids postoperatively. Peripheral nerve blocks on both sides of the upper abdomen are expected to be able to prolong the duration of pain relief, reduce the pain scale, and the total dose of pain medication needed postoperatively. The injection of this peripheral nerve block drug will be carried out by an anesthesiologist. Researchers will continue to anticipate the occurrence of side effects that can occur with strict monitoring and emergency care standards. This study will last up to 24 hours after surgery. The main question it aims to answer is: To prove that the amount of postoperative intravenous opioid consumption with M-TAPA block is lower than the control group.
Trial Details
NCT Number NCT06652581
Lead Sponsor Udayana University
Conditions Laparoscopic Cholecystectomy, Peripheral Nerve Block
Enrollment 42 participants
Start Date 2024-09-12
Primary Completion 2024-11-12 (estimated)
Study Completion 2024-11-13 (estimated)
Updated on ClinicalTrials.gov 2024-10-22