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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: ChiCTR
Last refreshed on: 16 October 2023
Main ID:  ChiCTR2200057381
Date of registration: 2022-03-10
Prospective Registration: No
Primary sponsor: Peking University Third Hospital
Public title: Efficacy and safety of low-dose rituximab in the treatment of membranous nephropathy
Scientific title: Efficacy and safety of low-dose rituximab in the treatment of membranous nephropathy
Date of first enrolment: 2022-03-01
Target sample size: rituximab group:68;control:135;
Recruitment status: Pending
URL:  https://www.chictr.org.cn/showproj.html?proj=153418
Study type:  Observational study
Study design:  Cohort study  
Phase:  N/A
Countries of recruitment
China
Contacts
Name: Danxia Zheng   
Address:  49 Huayuan North Road, Haidian District, Beijing 100191
Telephone: +86 13522758603
Email: dxheng@sina.com
Affiliation:  Peking University Third Hospital
Name: Danxia Zheng   
Address:  49 Huayuan North Road, Haidian District, Beijing 100191
Telephone: +86 13522758603
Email: dxheng@sina.com
Affiliation:  Peking University Third Hospital
Key inclusion & exclusion criteria
Inclusion criteria: 1. Clinical diagnosis of nephrotic syndrome;
2. Renal biopsy for diagnosis of IMN;
3. Blood PLA2R antibody>20IU/ml;
4. Age: 18-80 (inclusive), regardless of gender;
5.eGFR>30 ml/min.

Exclusion criteria: 1. Renal pathology indicates that in addition to IMN, there are also other kidney diseases, such as diabetes nephropathy;
2. Secondary IMN, such as systemic lupus erythematosus, chronic hepatitis B, tuberculosis, tumor, etc.


Age minimum: 18
Age maximum: 80
Gender: Both
Health Condition(s) or Problem(s) studied
membranous nephropathy
Intervention(s)
rituximab group:rituximab;control:hormone combined with cyclophosphamide;
Primary Outcome(s)
nephrotic syndrome outcome;renal function;
Secondary Outcome(s)
complications;
Secondary ID(s)
Source(s) of Monetary Support
Peking University third Hostipal
Secondary Sponsor(s)
Ethics review
Status: Approved
Approval date: 03/03/2022
Contact:
Liang Lijun
+86 10 82265883
Results
Results available:
Date Posted:
Date Completed:
URL:
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