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Effect of Febuxostat on vascular function in patients with hyperuricemia

Not Applicable
Conditions
hyperuricemia
Registration Number
JPRN-UMIN000009468
Lead Sponsor
agasaki University Graduate School of Biomedical Sciences Department of Cardiovascular Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
30
Inclusion Criteria

Not provided

Exclusion Criteria

The patients who meet the following criteria are excluded; 1)Patients will not take Febuxostat or Benzbromarone more than three months. 2)Frequent changes of concomitant medications are expected. 3)Patients with severe renal failure(eGFR<30 mL/min/1.73m2) and/ or on dialysis. 4)Pregnant woman 5)Patients have problems of severe allergic diseases on clinical course, or have a history of serious side effects and/or hypersensitivity to these drugs. 6)The physician judges that patients are inappropriate to attend this study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change of RHI measured by EndoPAT
Secondary Outcome Measures
NameTimeMethod
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