Clin2
NCT07581275Possibly a fitNot yet recruiting

Levobupivacaine levels after TAP block for abdominal surgery

Abdominal Surgery PatientsTransversus Abdominis Plane (TAP) BlockPharmacokinetic AnalysisLevobupivacaineLocal Anaesthetic Systemic Toxicity

Part of Injuries & trauma clinical trials.

This study looks at how a numbing medicine called levobupivacaine stays in your body after a pain-blocking injection in your belly wall during abdominal surgery. It may help doctors give better pain relief with fewer side effects.

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

Phase
N/A
Enrollment
26 people
Ages
18 years to 75 years
Study type
Observational

Who can take part

  • You are 18 years or older
  • You are having planned (non-emergency) abdominal surgery under general anesthesia
  • You will receive a TAP block (an ultrasound-guided numbing injection in your belly) as part of your pain care
  • You can read and understand French well enough to review the study details and sign a consent form
  • You do not have liver or kidney problems, allergies to similar numbing medicines, or any condition that would make blood draws difficult
  • You are not pregnant

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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