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NCT06488183Possibly a fitRecruiting

Pain relief study for laparoscopic weight loss surgery

Pain Management

Part of Brain & nervous system clinical trials.

This study compares two ways to manage pain after laparoscopic bariatric surgery: one method involves numbing medicine placed near the surgery site, and the other uses an ultrasound-guided injection near the back. It aims to find which option works better for recovery in people with moderate to severe obesity.

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

Phase
N/A
Enrollment
44 people
Ages
20 years to 50 years
Study type
Interventional

Who can take part

  • You are between 20 and 50 years old.
  • You are scheduled for laparoscopic bariatric surgery.
  • You have a body mass index (BMI) between 35 and 50.
  • You are in generally good health (classified as ASA I, II, or III).
  • You do not have severe heart disease, chronic kidney failure, or liver cirrhosis.
  • You are not allergic to bupivacaine (a numbing medication).
  • You do not regularly use strong pain medicines (opioids) for a long time.

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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