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NCT06696248Possibly a fitNot yet recruiting

Testing carvedilol and alverine for liver cirrhosis with high blood pressure in the portal vein

Hypertension, Portal

Part of Digestive system clinical trials.

This trial is for people with liver cirrhosis who already take carvedilol for portal hypertension (high blood pressure in the liver's main vein). It tests whether adding alverine helps lower that pressure more effectively.

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

Phase
Phase 2/Phase 3
Enrollment
30 people
Ages
18 years to 80 years
Study type
Interventional

Who can take part

  • You are between 18 and 80 years old.
  • You have been diagnosed with liver cirrhosis (a scarring of the liver).
  • You have been taking carvedilol for at least 3 months, at a dose up to 15 mg per day (or the highest dose you can handle).
  • You have not taken alverine, papaverine, or similar medicines in the last 4 weeks.
  • You have not had a transjugular intrahepatic portosystemic shunt (TIPS) or other procedure that lowers portal pressure, and you have not had a liver transplant.
  • You can avoid heavy drinking (more than 1–2 drinks a day) for at least 12 weeks before and during the study.

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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