Clinical Trials Directory

Trials / Completed

CompletedNCT00801463

Prednisone Plus Tripterygium Wilfordii Treatment of Adult Patients With Idiopathic Focal Segmental Glomerulosclerosis

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
67 (actual)
Sponsor
Nanjing University School of Medicine · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to assess the efficacy of prednisone and tripterygium wilfordii in treated Focal Segmental Glomerulosclerosis (FSGS).

Detailed description

Primary FSGS is a leading cause of end stage renal disease in adults, with complete loss of kidney function in 50% of patients over 10 years. Steroids, which are currently used to treat the disease, are effective in part of patients. Over the past decade, a number of studies have reported therapeutic efficacy for treatment with high-dose and over 6mo prednisone in patients with FSGS. These studies show that the total effective rates were only around 50%. But this therapy had taken some side effects of prednisone. Except these studies, in recent studies suggest that Tripterygium Wilfordii may be effective for passive Heymann nephritis, podocyte injury in nephrosis rats induced y puromycin aminonucleoside, and so on. FSGS is a podocytepathy. There was no-data of Prednisone and Tripterygium Wilfordii treatment of Chinese adult patients with idiopathic FSGS.

Conditions

Interventions

TypeNameDescription
DRUGtripterygium wilfordii (TW)Pre 30mg/d +TW 120 mg/d, po for 12 weeks

Timeline

Start date
2009-01-01
Primary completion
2011-01-01
Completion
2011-02-01
First posted
2008-12-03
Last updated
2011-05-18

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT00801463. Inclusion in this directory is not an endorsement.