Treatment of Hyperuricemia in Patients With Heart Failure

NCT ID: NCT00422318

Last Updated: 2007-01-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Study Classification

INTERVENTIONAL

Study Start Date

2004-01-31

Study Completion Date

2005-12-31

Brief Summary

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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

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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.

Conditions

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Heart Failure Hyperuricemia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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Benzbromarone (drug)

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* chronic heart failure
* hyperuricemia

Exclusion Criteria

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

ALL

Accepts Healthy Volunteers

No

Sponsors

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Tottori University Hospital

OTHER

Sponsor Role lead

Principal Investigators

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Kazuhide Ogino, MD

Role: PRINCIPAL_INVESTIGATOR

Tottori University Hospital

Locations

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Tottori University Hospital

Yonago, , Japan

Site Status

Countries

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Japan

References

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Ogino K, Kato M, Furuse Y, Kinugasa Y, Ishida K, Osaki S, Kinugawa T, Igawa O, Hisatome I, Shigemasa C, Anker SD, Doehner W. Uric acid-lowering treatment with benzbromarone in patients with heart failure: a double-blind placebo-controlled crossover preliminary study. Circ Heart Fail. 2010 Jan;3(1):73-81. doi: 10.1161/CIRCHEARTFAILURE.109.868604. Epub 2009 Nov 20.

Reference Type DERIVED
PMID: 19933411 (View on PubMed)

Other Identifiers

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#345

Identifier Type: -

Identifier Source: org_study_id

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