Overview

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

Status:
Completed
Trial end date:
2011-02-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to assess the efficacy of prednisone and tripterygium wilfordii in treated Focal Segmental Glomerulosclerosis (FSGS).
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Nanjing University School of Medicine
Treatments:
Prednisone
Criteria
Inclusion Criteria:

- Age 18-60 years at onset of signs or symptoms of FSGS

- Urine protein ≥ 3.5 g/24 h

- Estimated glomerular filtration rate (GFR) ≥ 40 ml/min/1.73 m2, serum
creatinine<2.5mg/dl

- Biopsy confirmed as idiopathic FSGS (including all subtypes)

- Willingness to follow the clinical trial protocol, including medications, and baseline
and follow-up visits and procedures

Exclusion Criteria:

- Secondary FSGS

- Prior therapy with sirolimus, Cyclosporine, MMF, azathioprin, cytoxan, chlorambucil,
levamisole, methotrexate, or nitrogen mustard in the last 90 days

- Active/serious infection

- Malignancy

- Previously diagnosed as diabetes mellitus type 1 or 2, or abnormal carbohydrate
tolerance

- Peripheral white blood cells < 3000/ul

- Clinical evidence of cirrhosis or chronic active liver diseases

- History of significant gastrointestinal disorder

- Allergy to study medications, and Inability to consent/assent