Clinical trial Recruiting at 2 sites Phase 4 Interventional Ages 18 to 70

Allopurinol to prevent complications in decompensated liver cirrhosis

Official title: Role of Allopurinol in Prevention of Complications Related to Decompensated Cirrhosis of Liver'

Run by Bangladesh Medical University · NCT07800598 · Data updated 2026-11-12

This trial tests whether allopurinol can reduce complications in adults with decompensated cirrhosis.

More Decompensated Cirrhosis trials

Quick facts

PhasePhase 4
Study typeInterventional
Ages18 Years to 70 Years
SexAll
Enrollment54 (estimated)
SponsorBangladesh Medical University
Academic / other
Drugs / interventionsCyclophosphamide
Locations2 sites (Dhaka, Shahbagh and 1 other locations)
StatusRecruiting
StartedSeptember 10, 2025
Main results expectedDecember 2026
Study endsJuly 2027
Registry record updatedSeptember 2, 2026
Trial IDNCT07800598 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18-70 with decompensated cirrhosis (Child-Pugh B or C) of any etiology.

Probably not a fit

Patients with active hepatic encephalopathy, spontaneous bacterial peritonitis, hepatorenal syndrome, or severe renal impairment may not benefit and are excluded.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This phase 4 interventional study will evaluate the effect of allopurinol versus placebo on complications of decompensated cirrhosis in adults aged 18-70 with Child-Pugh B or C scores. Participants will be randomly assigned to receive allopurinol or placebo and will be monitored for cirrhosis-related events such as ascites, variceal bleeding, hepatic encephalopathy, spontaneous bacterial peritonitis, and hepatorenal syndrome with acute kidney injury, as well as changes in MELD and Child-Pugh scores. The trial aims to generate robust clinical evidence on whether allopurinol can reduce complications and improve liver disease severity. Eligibility includes adults with decompensated cirrhosis, whereas those with active HE/SBP/HRS-AKI, significant renal impairment, pregnancy, or allopurinol hypersensitivity are excluded. Conduct is centered at the Department of Hepatology, Bangladesh Medical University, Dhaka.

Why it matters

Potential benefit: If successful, patients could experience fewer liver-related complications and potential improvement in liver disease severity scores.

How similar studies have gone: Prior evidence with allopurinol in cirrhosis is promising but robust randomized data are limited; this study seeks to provide more definitive results.

Who can join: the full rules

Show full inclusion / exclusion criteria
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 ).

Where it's running

  • Department of Hepatology at Bangladesh Medical University.
    Dhaka, Shahbagh, Bangladesh
    Recruiting
  • Department of Hepatology at Bangladesh Medical University.
    Dhaka, Bangladesh
    Recruiting

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.