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Treatment of Hyperuricemia in Patients With Heart Failure

Hyperuricemia and the Effects of the Uricosuric Agents Benzbromarone in Patients With Chronic Heart Failure

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00422318
Enrollment
Unknown
Registered
2007-01-15
Start date
2004-01-31
Completion date
2005-12-31
Last updated
2007-01-15

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

Conditions

Heart Failure, Hyperuricemia

Keywords

Heart Failure, Insulin, Metabolism, Pharmacology, Uric Acid

Brief summary

The study aims to assess (I) the contribution of UA itself to the CHF pathophysiology and (II) to test the effect of lowering UA by uricosuric treatment in CHF.

Detailed description

Hyperuricemia is often observed in patients with congestive heart failure (CHF). It has been reported that hyperuricemia is related to exercise capacity, inflammation markers and diastolic dysfunction in such patients. In addition, hyperuricemia in CHF relates to both symptomatic status (i.e. morbidity) as well as impaired prognosis (i.e. mortality). Hyperuricemia is likely to play an important role in the pathophysiology of CHF. Up-regulation of xanthine oxidase (XO) activity in CHF has been shown to contribute to higher uric acid (UA) in CHF and the therapeutic concept of XO inhibition has shown beneficial effects in a number of surrogate markers in these patients. The XO inhibition accounts for substantial decrease in oxygen radical load, the latter is discussed as the main benefit of XO inhibition treatment in hyperuricemic patients. However, whether high uric acid itself is important or merely a marker of XO activity (and hence of increased radical accumulation) is currently under discussion. Therefore, this study aims to assess (I) the contribution of UA itself to the CHF pathophysiology and (II) to test the effect of lowering UA by uricosuric treatment in CHF.

Interventions

DRUGBenzbromarone (drug)

Sponsors

Tottori University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL

Inclusion criteria

* chronic heart failure * hyperuricemia

Exclusion criteria

* renal dysfunction (Cr \> 2.0 mg/dl) * under treatment with anti-diabetic agents

Design outcomes

Primary

MeasureTime frame
parameters of echocardiography at 16 weeks
BNP levels at 16 weeks

Secondary

MeasureTime frame
parameters of glucose metabolism at 16 weeks
Parameters of lipid metabolism at 16 weeks

Countries

Japan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 1, 2026