Clin2
NCT06737341Likely a fitRecruiting

Liposomal vs. Standard Bupivacaine for Pain after Keyhole Abdominal Surgery

BupivacaineUltrasound-GuidedAnalgesia, PostoperativeOpioids

Treatments studied

Part of Brain & nervous system clinical trials.

This trial tests whether a long-acting numbing medicine (liposomal bupivacaine) works better than standard bupivacaine to control pain after keyhole surgery on the liver, bile ducts, or pancreas. It may help you experience less pain and need fewer painkillers after surgery.

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

Phase
Phase 4
Enrollment
60 people
Ages
18 years to 80 years
Study type
Interventional

Who can take part

  • You are between 18 and 80 years old.
  • Your overall health status is ASA I, II, or III (generally healthy to moderate illness).
  • You are having laparoscopic (keyhole) surgery on your liver, bile ducts, or pancreas.
  • Your body mass index (BMI) is between 15 and 30.
  • You do not have a known history of alcohol or drug abuse.
  • You have not had previous upper abdominal surgery, bleeding disorders, infections, or nerve problems (peripheral neuropathy).

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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