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Recruiting NCT07064200

TAP Block Timing Study

Trial Parameters

Condition Bariatric or General Abdominal Surgeries
Sponsor Weill Medical College of Cornell University
Study Type INTERVENTIONAL
Phase N/A
Enrollment 150
Sex ALL
Min Age 18 Years
Max Age 65 Years
Start Date 2025-07-14
Completion 2026-12-01
Interventions
TAP Block

Brief Summary

This study investigates whether administering TAP blocks pre-incision provides superior postoperative pain control and reduces opioid use along with other medications compared to post-incision administration in patients undergoing elective abdominal surgeries.

Eligibility Criteria

Inclusion Criteria: * Adults aged between 18 and 65 years * Scheduled for elective bariatric surgery or other elective general abdominal surgeries * Proficient in English sufficient to understand study procedures and communicate effectively * Capable of providing informed consent Exclusion Criteria: * Individuals under 18 years of age (minors) * Pregnant individuals * Prisoners * Individuals with cognitive impairments or otherwise unable to provide informed consent independently * Individuals with known allergies or contraindications to local anesthetics used in TAP blocks

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