Clinical Trials Directory

Trials / Completed

CompletedNCT00426348

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

A Prospective Randomized, Controlled, Double Blinded Trial of the Antioxidant Probucol Combined With Valsartan in Patients With IgA Nephropathy

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
75 (actual)
Sponsor
Guangdong Provincial People's Hospital · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGValsartanValsartan (80-160mg/day)
DRUGProbucolProbucol (750mg/day)
DRUGPlaceboPlacebo

Timeline

Start date
2007-05-01
Primary completion
2013-01-01
Completion
2013-01-01
First posted
2007-01-24
Last updated
2013-08-28

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT00426348. Inclusion in this directory is not an endorsement.