Clin2
NCT07876297Possibly a fitNot yet recruiting

Numbing medicine placement for abdominal surgery pain relief

Cutaneous Sensory Blockade

Part of Brain & nervous system clinical trials.

This study tests how different amounts and locations of numbing medicine (rectus sheath block) affect pain relief and sensation after laparoscopic abdominal surgery. It may help patients have better pain control with fewer side effects.

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

Phase
N/A
Enrollment
120 people
Ages
20 years and older
Study type
Interventional

Who can take part

  • You are scheduled for laparoscopic (keyhole) surgery on your upper or lower belly, including some urological procedures
  • You are in good general health (classified as ASA I-III by your anesthesia doctor)
  • You are 20 years or older
  • You weigh at least 50 kg (about 110 pounds)
  • You have not had abdominal surgery before
  • You are not morbidly obese (BMI less than 40)
  • You do not have severe liver disease, bleeding disorders, nerve problems, kidney failure, chronic pain, or drug addiction
  • You are not allergic to bupivacaine (a common numbing medicine)

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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