Clin2
NCT07581275Possibly a fitNot yet recruiting

Pain Relief Medication Levels After Abdominal Surgery

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

Part of Injuries & trauma clinical trials.

This study measures how a pain-relief medication (levobupivacaine) enters and moves through your bloodstream after you receive a nerve block injection during planned abdominal surgery. The findings may help doctors understand the best way to use this medication for pain control.

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 (not emergency) abdominal surgery under general anesthesia
  • Your surgery plan already includes an ultrasound-guided nerve block (TAP block) for pain relief
  • You can speak and understand French well enough to give informed consent
  • You have no severe liver or kidney problems
  • You are willing to have multiple blood samples taken during the study period

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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