TAP Block Timing Study for Abdominal Surgeries

This study is looking at whether the timing of a TAP block (a type of pain relief injection for the belly area) makes a difference for people having bariatric or other general abdominal surgeries. Researchers want to see if getting the TAP block before surgery starts helps more with pain and reduces the need for opioid pain medications compared to getting it after surgery starts. You might be able to join if you are between 18 and 65 years old, are scheduled for one of these surgeries, and can understand English. The study will measure how much opioid medication you use and your pain levels for up to 90 days after your surgery. The current status of this study is unclear.

Study design
This interventional study plans to enroll 150 participants. It compares two different timings for receiving a TAP block.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Your opioid use will be tracked for up to 90 days after surgery, and your pain scores will be checked at several points up to 72 hours post-surgery.

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NCT07064200

TAP Block Timing Study

Recruiting
NAAges 18–65InterventionalTreatment
Weill Medical College of Cornell University
~150 participants
Updated 2026-01-27 on ClinicalTrials.gov
What's tested:TAP Block

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Mean change in opioid consumption (MME) from index procedure to 90 days post-op
Measured over Up to 90 days post-operatively
+1 more outcome measured
Bariatric or General Abdominal Surgeries
Bariatric Surgery Patients
1 sites across 1 states
New York1
  • Cheguevara Afaneh, MD · PRINCIPAL_INVESTIGATOR · Weill Medical College of Cornell University

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Eligibility criteria

Inclusion

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

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
  • Mean change in opioid consumption (MME) from index procedure to 90 days post-opUp to 90 days post-operatively

    Opioid dosage quantities will be measured in morphine milligram equivalents (MME)

  • Change in Pain Scores from index procedure on a numerical rating scale1, 3, 6, 24, 48, and 72 hours postoperatively

    Patient-reported pain on a scale of 1-10.