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The study of the safety and effect of high dose allopurinol in patients with severe heart failure

The study of the safety and effect of high dose allopurinol on the clinical, laboratory and echocardiographic variables in patients with severe left ventricle systolic dysfunction

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015112125171N1
Enrollment
30
Registered
2016-05-23
Start date
2016-02-28
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart failure.

Interventions

Using 600 mg allopurinol daily for 3 months.
Treatment - Drugs
Using 600 mg allopurinol daily for 3 months

Sponsors

Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age of 18-80 years old; severe left ventricle systolic dysfunction (Ejection fraction of less than 35%) on optimal medical treatment for at least one month with New York heart association functional class of II-III; having informed written consent. Exclusion criteria: Below the age of 18 and above the age of 80 years old; glomerular filtration rate of less than 60ml/min; serum creatinine level of more than 3mg/dl; severe hepatic failure; use of azathioprin; use of 6mercaptopurin; use of warfarin; known history of sensitivity to allopurinol.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
ProBNP. Timepoint: 3 month. Method of measurement: Laboratory kit.;6 minute walk test. Timepoint: 3 month. Method of measurement: Rehabilitation department of the center.;Strain echocardiography. Timepoint: 3 month. Method of measurement: Vivid 6s echocardiography system.;Quality of life of the patients. Timepoint: 3 month. Method of measurement: IHF-QoL.

Secondary

MeasureTime frame
Skin rash. Timepoint: during the 3 months. Method of measurement: Medical history and physical exam.;Gastrointestinal compliations. Timepoint: during the 3 months. Method of measurement: Medical history and physical exam.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Mostafa Ansari-Ramandi

Rajaie Cardiovascular Medical and Research Center. Tehran, Iran

dr_mm_ansari@yahoo.com+98 21 8823 3597

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026