Intravenous Allopurinol in Heart Failure
Completed · Phase 2 · Has a placebo group
Conditions studied: Congestive Heart Failure
In brief
This study tests the hypothesis that allopurinol, a xanthine oxidase inhibitor, improves heart metabolism in patients with heart failure.
Key facts
- Study ID
- NCT00181155
- Run by
- Johns Hopkins University
- People needed
- 18
- Starts
- 2004-11-01
- Expected to finish
- 2010-12-01
- Last updated by the study team
- 2017-05-30
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age > 18 years
- The patient is willing and able to provide informed consent
- Clinical diagnosis of chronic heart failure
- Ejection fraction (EF) < 40% by echocardiography, nuclear multigated acquisition (MUGA) or cath ventriculography
- No significant coronary disease at cardiac catheterization
- New York Heart Association (NYHA) Class I-IV symptoms
- Clinical stabilization for two weeks if following recent congestive heart failure (CHF) decompensation.
You may not qualify if…
- Metallic implant prohibiting magnetic resonance (MR) evaluation
- Inability to lie flat for MR study
- Administration of additional investigational drugs
- Calculated creatinine clearance < 50 mL/min
- Allergy to allopurinol
- Current gout flare
- Currently taking oral allopurinol
Where it is running
- Johns Hopkins Hospital — Baltimore, Maryland, United States
Full record on ClinicalTrials.gov
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