Clin2
NCT07518238Likely a fitEnrolling by invitation

Pain Relief Methods for Abdominal Wall Surgery

BDE for Hernia PatientsExparel for Hernia Patients

Part of Digestive system clinical trials.

This study compares two different pain-relief injection techniques (BDE and Exparel) given during abdominal wall reconstruction surgery to see which works better at reducing pain and opioid use after surgery. You would receive one of these injections as part of your anesthesia care.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 2
Enrollment
128 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are having robotic or open abdominal wall reconstruction surgery at a BSW Health facility
  • You are 18 years or older
  • You are not pregnant (women of childbearing age will have a pregnancy test before surgery)
  • You have not had chronic pain or do not regularly take opioid pain medications
  • You are not allergic to BDE, Exparel, acetaminophen, gabapentin, or pregabalin
  • You are not having any other surgeries planned during the same hospital stay

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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