Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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19 February 2015 |
Main ID: |
NCT00404833 |
Date of registration:
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27/11/2006 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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Mycophenolate Mofetil in Membranous Nephropathy and Focal Segmental
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Scientific title:
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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) |
Date of first enrolment:
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January 2003 |
Target sample size:
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16 |
Recruitment status: |
Completed |
URL:
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http://clinicaltrials.gov/show/NCT00404833 |
Study type:
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Interventional |
Study design:
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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Phase:
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Phase 3
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Countries of recruitment
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China
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Contacts
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Name:
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Daniel TM Chan, Prof |
Address:
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Telephone:
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Email:
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Affiliation:
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Department of Medicine, Queen Mary Hospital |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- abnormal urine protein excretion and biopsy-proven idiopathic membranous nephropathy
or focal segmental glomerulosclerosis
Age minimum:
18 Years
Age maximum:
65 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Glomerulosclerosis, Focal
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Glomerulonephritis, Membranous
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Intervention(s)
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Drug: prednisolone and mycophenolate mofetil
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Drug: prednisolone and chlorambucil
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Primary Outcome(s)
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Proteinuria
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Secondary Outcome(s)
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Adverse effects
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Secondary ID(s)
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HARECCTR0500005
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EC1838-02
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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