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Protective effects of Febuxostat in early chronic kidney disease

Protective effects of Febuxostat in early CKD: A Randomized Controlled Trial at a tertiary care centre - NIL

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/099694
Enrollment
177
Registered
2025-12-23
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Health Condition 1: N181- Chronic kidney disease, stage 1 Health Condition 2: N182- Chronic kidney disease, stage 2 (mild) Health Condition 3: N183- Chronic kidney disease, stage 3 (moderate)

Interventions

Intervention1: Placebo: Consisting of excipients only Intervention2: Febuxostat 40mg: To be given orally once daily for 3 months Control Intervention1: Febuxostat 20mg: To be given orally once daily f

Sponsors

Mohammad Shadab Ansari
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with Asymptomatic Hyperuricemia, with CKD stage 3 and below, attending Geneal Medicine/ Nephrology OPD and IPD Patients with Uric acid concentration 7 to 10 mg/dl Patients willing to give consent.

Exclusion criteria

Exclusion criteria: Patients with history of Gout. Patients with Alanine or Aspartate aminotransferase level more than 3-fold the upper limit defined at the institution. Patients on maintenance Hemodialysis therapy or Peritoneal dialysis. Patients with Kidney transplantation. Patients taking drugs like Thiazides or loop diuretics. Pregnant or lactating females Patients having received Uricosuric drugs in preceding 3 months.

Design outcomes

Primary

MeasureTime frame
Proportion of Patients showing more than 10 percent decline in eGFR in all 3 groupsTimepoint: Baseline to end of the study period

Secondary

MeasureTime frame
Changes in eGFR in the 3 groupsTimepoint: Baseline to end of the study period;Changes in Uric acid levels of the 3 groupsTimepoint: Baseline to end of the study period;Development of CKD stage 5Timepoint: Baseline to end of the study period;Any Cardiovascular eventsTimepoint: Baseline to end of the study period

Countries

India

Contacts

Public ContactMohammad Shadab Ansari

Jawaharlal Nehru Medical College

sfhalig@yahoo.co.in9412517518

Outcome results

None listed

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