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Study identifier: NCT07064200 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

TAP Block Timing Study

Condition: Bariatric or General Abdominal Surgeries · Bariatric Surgery Patients  ·  Sponsor: Weill Medical College of Cornell University

PhaseNA
Planned participants150
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Cheguevara Afaneh, MD  ·  +1 646 962 8462  ·  cha9043@med.cornell.edu

Hasan Ali  ·  hoa4002@qatar-med.cornell.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Weill Cornell Medical College - NewYork-Presbyterian HospitalNew York, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07064200