Clin2
NCT07263165Possibly a fitNot yet recruiting

Pain relief study for upper abdominal cancer surgery

Opioid Consumption, Postoperative

Treatments studied

Part of Pain clinical trials.

This study tests whether adding a sedative medicine to the numbing medication used in a nerve block can improve pain relief after upper abdominal cancer surgery. It may help reduce pain and the need for strong painkillers after the operation.

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

Phase
N/A
Enrollment
54 people
Ages
18 years to 70 years
Study type
Interventional

Who can take part

  • You are between 18 and 70 years old.
  • You are scheduled for surgery to remove a cancer in your upper abdomen (such as part of your stomach, liver, or pancreas).
  • You are in generally good health aside from the cancer (classified as ASA I-III).
  • Your body mass index (BMI) is between 18 and 35.
  • You are not allergic to local anesthetics or the sedative dexmedetomidine.
  • You do not have bleeding problems, infection at the injection site, or severe heart, lung, kidney, or liver disease.
  • You are not pregnant or breastfeeding.
  • You have not been taking strong painkillers (opioids) regularly for more than 3 months.

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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