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The urate-lowering efficacy and safety of febuxostat versus allopurinol in Chinese asymptomatic hyperuricemic patients with chronic kidney disease

The urate-lowering efficacy and safety of febuxostat versus allopurinol in Chinese asymptomatic hyperuricemic patients with chronic kidney disease

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-17011837
Enrollment
Unknown
Registered
2017-07-03
Start date
2017-07-06
Completion date
Unknown
Last updated
2017-07-10

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

Conditions

Hyperuricemia

Interventions

febuxostat group:febuxostat

Sponsors

the Affiliated Hospital of Qingdao University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Male and female aged 18 to 65 years; (2) patients with a diagnosis of and no history of renal replacement therapy; (3) patients with a diagnosis of HUA [sUA levels = 420 umol/L (7 mg/dL)in male and 360 umol/L in female]; (4) No urate lowering drugs were used before 1 month treatment.

Exclusion criteria

Exclusion criteria: 1. liver dysfunction (aspartate aminotransferase and/or alanine aminotransferase levels greater than two times the upper limit of institutional reference range); 2. gout, acute kidney injury, inflammatory disease, renal replacement therapy, active stage of peptic ulcer, malignancy, blood system disease, other serious disease; 3. received glucocorticoid/ immunosuppression therapy; 4. termination of treatment for personal reasons.

Design outcomes

Primary

MeasureTime frame
Serum uric acid;

Secondary

MeasureTime frame
estimated glomerular filtration rate;Proteinuria;

Countries

China

Contacts

Public ContactXuemei Liu

the Affiliated Hospital of Qingdao University

Liuxm2004@sina.com+86 18661807663

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026