Clinical Trials Directory

Trials / Completed

CompletedNCT00404833

Mycophenolate Mofetil in Membranous Nephropathy and Focal Segmental

A Prospective Randomized Open-label Study to Compare Mycophenolate Mofetil and Corticosteroid With Conventional Immunosuppressive Treatment on Proteinuria in Idiopathic Membranous Nephropathy (MN) and Focal Segmental Glomerulosclerosis (FSGS)

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
16 (estimated)
Sponsor
Hospital Authority, Hong Kong · Other Government
Sex
All
Age
18 Years – 65 Years
Healthy volunteers

Summary

This is a prospective randomized open-label pilot study to investigate the effect of mycophenolate mofetil treatment in patients with abnormal urine protein excretion due to membranous nephropathy (MN) or focal segmental glomerulosclerosis (FSGS). The change in urine protein excretion will be the primary outcome studied. The treatment regimen comprising prednisolone and mycophenolate mofetil will be compared with prednisolone and chlorambucil in MN, and compared with prednisolone in FSGS. The study duration will be 12 months for each patient.

Conditions

Interventions

TypeNameDescription
DRUGprednisolone and mycophenolate mofetil
DRUGprednisolone and chlorambucil

Timeline

Start date
2003-01-01
Completion
2006-12-01
First posted
2006-11-29
Last updated
2013-10-23

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT00404833. Inclusion in this directory is not an endorsement.