drugset / Trial / NCT00426348

A Study of the Antioxidant Probucol Combined With Valsartan in Patients With IgA Nephropathy

NCT00426348 ↗

Phase 4 Completed 75 enrolled Guangdong Provincial People's Hospital
RandomizedParallel-groupQuadruple-blindTreatment

Summary

a statement of the study hypothesis:the effect of valsartan in patients with IgA nephropathy have been proved,and the efficacy of probucol in combination with valsartan is to be proved in patients with IgA nephropathy. This is a prospective randomized controlled, double blinded pilot study to identify the efficacy of probucol in combination with valsartan in patients with IgA nephropathy. The renal function deterioration will be the primary outcome studied. The expected study duration will be 36 months.

Timeline

Start
2007-05
Primary completion
2013-01
Completion
2013-01

Outcome

Missed primary endpoint

paper The primary endpoint (doubling serum creatinine) showed no significant difference between the two groups during 3-year follow-up. PMID 24191893 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Probucol Small molecule 750 mg —
Background Valsartan Unknown 80 mg —
Background Valsartan Unknown 160 mg —