Can a common gout drug shield the liver from cirrhosis complications?
NCT ID NCT07800598
First seen Sep 02, 2026 · Last updated Sep 03, 2026 · Updated 1 time
Summary
This trial tests whether allopurinol, a drug usually used for gout, can prevent serious complications in people with decompensated cirrhosis, a late stage of liver disease. Researchers will give 54 adults with Child-Pugh B or C cirrhosis either allopurinol or a placebo for six months, alongside standard care. The goal is to see if allopurinol reduces events like fluid buildup, bleeding, and kidney failure, and improves liver function scores.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- allopurinol tablet
- What this could lead to
- If it works, allopurinol could become a low-cost, widely available way to prevent life-threatening complications in people with advanced cirrhosis.
- What could go wrong
- This is a small, early-phase trial with only 54 participants, so results may not apply broadly. Allopurinol can cause allergic reactions and is not safe for people with severe kidney problems.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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About 54 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2025
- Expected to finish
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Jul 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 70 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * • Adult patients (age : 18-70 years) diagnosed with Decompensated cirrhosis of liver with any etiology of cirrhosis . * CTP score B or C . Exclusion Criteria: * • Patients with known hypersensitivity or allergy to allopurinol. * Patients with active HE or SBP or HRS-AKI or a history of any of these events within the last 4 weeks. * Patients with advanced renal impairment (e.g., creatinine clearance \<30 mL/min). * Pregnant or breastfeeding women. * Patients with severe comorbidities (e.g., uncontrolled cardiovascular disease, cancer, or severe infections). * Patients currently using medications that interact with allopurinol (e.g., azathioprine, mercaptopurine, Cyclophosphamide, Thiazide diuretics ,Warfarin, Theophyllin ).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Department of Hepatology at Bangladesh Medical University.
RECRUITINGDhaka, Shahbagh, 1100, Bangladesh
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Department of Hepatology at Bangladesh Medical University.
RECRUITINGDhaka, Bangladesh
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