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The establishment of the effective treatment for hyperuricemia in hypertensive patient with hyperuricemia

The establishment of the effective treatment for hyperuricemia in hypertensive patient with hyperuricemia - The treatment for hyperuricemia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000010222
Enrollment
20
Registered
2013-03-12
Start date
2013-03-12
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

Interventions

1.febuxostat40mg 2.febuxostat20mg+benzbromarone25mg 3.benzbromarone50mg 1.benzbromarone50mg 2.febuxostat20mg+benzbromarone25mg 3.febuxostat40mg

Sponsors

National Cerebral and Cardiovascular Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: hypertensive patients with hyperuricemia, whose serum uric acid level >8 mg/dL on untreated or serum uric acid level >6 mg/dL in spite of taking UA lowering drugs over three months.

Exclusion criteria

Exclusion criteria: resistant hypertensive patient (SBP>=180mmHg or DBP>=110mmHg), heart failure patient (more than NYHA classification III or EF<=35%), severe renal damage patient (serum creatinine level >2 mg/dL), impaired liver function patient (AST or ALT>=100IU/ml), the patient with myocardial infarction, angina, and stroke within six months, an acute gouty attack patient, the patient with renal stone, the patient with taking mercaptopurine hydrate, azathioprine or warfarin, the patient with hypersensitivity to benzbromarone or febuxostat, patients to whom the doctor judged the participation in an examination to be unsuitable

Design outcomes

Primary

MeasureTime frame
serum uric acid, uric acid clearance, adverse event

Secondary

MeasureTime frame
blood pressure. renal function, oxidant stress, endothelial function, renal artery resistance, inflammation

Countries

Japan

Outcome results

None listed

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