TAP Block Timing Study

Recruiting N/A Interventional Study
Bariatric or General Abdominal Surgeries Bariatric Surgery Patients
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 65
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
150 (estimated)
Sponsor
Weill Medical College of Cornell University · Other
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About This Trial

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.

Trial Locations
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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 Criteri…
Contacts

Cheguevara Afaneh, MD

+1 646 962 8462

cha9043@med.cornell.edu

CONTACT

Hasan Ali

hoa4002@qatar-med.cornell.edu

CONTACT