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A randomized trial to evaluate the cardioprotective effect of the uric acid-lowering therapy for hyperuricemia in patients with chronic heart failure

A randomized trial to evaluate the cardioprotective effect of the uric acid-lowering therapy for hyperuricemia in patients with chronic heart failure - A randomized trial to evaluate the cardioprotective effect of uric acid-lowering therapy for hyperuricemia in patients with chronic heart failure

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-C000000426
Enrollment
60
Registered
2006-06-01
Start date
2006-06-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Hyperuricemia in patients with chronic heart failure

Interventions

Benzbromarone (25-75 mg daily) for 4 months Allopurinol (100-300mg daily) for 4 months Life-style modification

Sponsors

National Cardiovascular Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The patients who have stable left ventricular systolic dysfunction (fractional shortening <25%) and hyperuricemia (serum uric acid >=8.0 mg/dl)

Exclusion criteria

Exclusion criteria: 1) Gouty arthritis or tophus 2) Patients who have already taken the uric acid-lowering drugs 3) Renal dysfunction (serum creatinin >=2.0 mg/dl) 4) Urinary or renal calculus 5) Hepatic dysfunction (GPT (ALT) >=50 IU/l) 6) Patients who do not agree and whom physician judges inappropriate to this trial for any reason

Design outcomes

Primary

MeasureTime frame
1) The plasma BNP levels 2) The plasma levels of markers of oxidative stress 3) The plasma levels of pro-inflammatory cytokines

Secondary

MeasureTime frame
1) NYHA functional class 2) Hospitalizaion for worsening heart failure

Countries

Japan

Contacts

Public ContactMasanori Asakura

National Cardiovascular Center Cardiovascular Clinical Research Center

asamasa@xd5.so-net.ne.jp06-6833-5012

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026