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The urate-lowering efficacy and safety of febuxostat in the treatment of the hyperuricemia in chronic kidney disease.

The urate-lowering efficacy and safety of febuxostat in the treatment of the hyperuricemia in chronic kidney disease. - The effects and safety of febuxostat in chronic kidney disease.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000005573
Enrollment
40
Registered
2011-05-16
Start date
2011-05-01
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

Hyperuricemic patients with CKD

Interventions

1)Febuxostat group CKD patients with hyperuricemia (Uric acid more than 6mg/dl) are scheduled to treat with 10 mg/day of febuxostat in the beginnings. The doses of febxostat are allowed to increase u

Sponsors

Yokohama City University Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)adult(older than 19 years-old) 2)regardless of gender 3)Uric acid equal and more than 8mg/dl and the eGFR of less than 60ml/min/1.73m2 4)The general condition of the participants need to be stable. The participants should be treated according to the CKD practice guideline except uric acid treatment 5) Written informed consent should be obtained by all participants.

Exclusion criteria

Exclusion criteria: 1.The patients who are contraindicated to use febuxostat or allopurinol. 1)Patients who have liver injury(The ALT more than 200 IU/L) 2) Woman who is pregnat. 3) Patients who have allergy to febuxostat or allopurinol. 2. Patients who are judged as inadequate to participate the study by the their doctors.

Design outcomes

Primary

MeasureTime frame
1) Serum Uric acid 2) Serum Cr, eGFR 3) Derum systatin C

Secondary

MeasureTime frame
1) Urinary protein/Cr ratio 2) Urinary tubular markers/Cr ratio 3) Urinary uric acid excretion ratio

Countries

Japan

Contacts

Public ContactNobuhito Hirawa

Yokohama City University Medical Center Department of hemodialysis and apheresis

hirawa@yokohama-cu.ac.jp045-261-5656

Outcome results

None listed

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