RecruitingPhase 2NCT06270147

Timing of TAP Blocks in Bariatric Surgery

Single Blind Clinical Trial: Optimizing TAP Block Timing for Bariatric Surgery


Sponsor

McMaster University

Enrollment

100 participants

Start Date

Nov 21, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This clinical trial aims to determine the optimal timing for administering a Transversus Abdominis Plane (TAP) block in bariatric surgery, specifically investigating whether initiating TAP blocks at the beginning of surgery is more beneficial than at the end, which is the current practice. The study targets obese patients undergoing bariatric surgery, with a focus on reducing postoperative pain and opioid use. Key outcomes include recovery duration, pain levels, opioid consumption, and respiratory function. Successful results could establish early TAP block initiation as a standard practice, offering faster recovery, decreased opioid reliance, and reduced healthcare costs.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Bupivacaine-epinephrine for people with opioid use and pain, postoperative. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years and older.

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

DRUGBupivacaine-epinephrine

A total of 60ml of 0.25% Bupivacaine with Epinephrine, divided into 4 aliquots, will be administered laparoscopically at two locations per side along the anterior axillary line between the costal margin and the iliac crest. TAP block timing will be disclosed to the operating surgeon to ensure the correct solution is administered at the appropriate time.


Locations(1)

St. Joseph's Healthcare Hamilton - Charlton Campus

Hamilton, Ontario, Canada

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NCT06270147


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