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Effect of Xanthine Oxidase inhibitor on the progression of CKD by controlling the asymptomatic hyperuricemia: a prospective, multicenter, open-label, randomized, controlled trial

Effect of Xanthine Oxidase inhibitor on the progression of CKD by controlling the asymptomatic hyperuricemia: a prospective, multicenter, open-label, randomized, controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-16008960
Enrollment
Unknown
Registered
2016-08-02
Start date
2016-11-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Chronic kidney disease

Interventions

intervention:drug
control group:no intervention

Sponsors

Tianjin First Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. According to the chronic kidney disease (CKD) diagnostic criteria of 2012 KDIGO; 2. Male and Female; 3. Aged 20-75 years old; 4. CKD 3b-4: eGFR 15~45 mL/min/1.73m2; 5. No history of gout; 6. Serum uric acid =6.5 mg/dL; 7. No history of gastrointestinal disease, can take the lowering uric acid drug.

Exclusion criteria

Exclusion criteria: 1. Acute kidney disease, nephrotic syndrom, obstructive nephropathy, and other unstable patients; 2. Have taken the hemodialysis, peritoneal dialysis or kidney transplantation; 3. Pregnancy or nursing during the study; 4. Maligant tumor; 5. Hypersensitivity to Febuxostat; 6. Intake mercaptopurine, azathioprine; 7. Intake following drugs before the trial within 4 weeks: Febuxostat, allopurinol, benzbromarone, probenecid, uricase; 8. Intake within 4 weeks: losartan, fenofibrate, diuretics; 9. Hormone replacement with estrogens; 10. Undertake other clinical trial within three months; 11. Other unsuitable reasons.

Design outcomes

Primary

MeasureTime frame
glomerular filtration rate;

Countries

China

Contacts

Public ContactChang Wenxiu

Tianjin First Central Hospital

changwx@sina.com+86 13512999628

Outcome results

None listed

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