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Effect of Topiroxostat on Urinary Albumin in hyperuricemic patients with Diabetic nephropathy

Phase 4
Conditions
Diabetic nephropathy with hyperuricemia
Registration Number
JPRN-UMIN000015403
Lead Sponsor
Department of Nephrology, Nagoya University Graduate School of Medicine
Brief Summary

The changes in UACR after 24 weeks of treatment (or at the final time point if patients failed to reach 24 weeks) relative to the baseline were -122 mg/gCr (95% CI: -5.1 to -240.1, P = 0.041) in patients treated with high dose, while treatment with low dose topiroxostat could not show significant reduction (P = 0.067).

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
80
Inclusion Criteria

Not provided

Exclusion Criteria

1 Poor diabetic control 2 Patient have been treated with steroids 3 Patient with nephropathy excluding diabetic nephropathy (including: nephrosclerosis) 4 Cancer 5 Systemic disease with proteinuria (collagen disease, vasculitis and amyloidosis) 6 Gouty arthritis within 6 months 7 ALT, AST >= double as the standard of each hospital 8 Active Hepatitis C and/or C 9 Liver cirrhosis 10 Patients are deemed unsuitable by a physician

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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