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.
Quick facts
| Phase | Phase 4 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years to 70 Years |
| Sex | All |
| Enrollment | 54 (estimated) |
| Sponsor | Bangladesh Medical University Academic / other |
| Drugs / interventions | Cyclophosphamide |
| Locations | 2 sites (Dhaka, Shahbagh and 1 other locations) |
| Status | Recruiting |
| Started | September 10, 2025 |
| Main results expected | December 2026 |
| Study ends | July 2027 |
| Registry record updated | September 2, 2026 |
| Trial ID | NCT07800598 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
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.