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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: 26 November 2018
Main ID:  ChiCTR1800019606
Date of registration: 2018-11-19
Prospective Registration: Yes
Primary sponsor: The First Affiliated Hospital of Chengdu Medical College
Public title: Effect of kunxian capsule and leflunomide on IgA nephropathy
Scientific title: Effect of kunxian capsule and leflunomide on IgA nephropathy
Date of first enrolment: 2018-12-01
Target sample size: 1:20;2:20;
Recruitment status: Pending
URL:  http://www.chictr.org.cn/showproj.aspx?proj=30728
Study type:  Interventional study
Study design:  Quasi-randomized controlled  
Phase:  Post-market
Countries of recruitment
China
Contacts
Name: FAN JUNMING   
Address:  278 Central Section of Baoguang Road, Xindu District, Chengdu, Sichuan, China
Telephone: +86 13908199530
Email: junmingfan@163.com
Affiliation:  The First Affiliated Hospital of Chengdu Medical College
Name: ZHENG YUNHENG   
Address:  278 Central Section of Baoguang Road, Xindu District, Chengdu, Sichuan, China
Telephone: +86 18782582608
Email: 18782582608@163.com
Affiliation:  The First Affiliated Hospital of Chengdu Medical College
Key inclusion & exclusion criteria
Inclusion criteria: 1. Renal biopsy proved to be IgA nephropathy;
2. aged 15~75 years old;
3. According to the KDIGO guidelines, patients with IgA nephropathy do not need to use glucocorticoid and immunosuppressive agents;
4. Volunteer for clinical trials and sign informed consent.

Exclusion criteria: 1. Combined with other immune diseases;
2. Allergic to this drug;
3. Acute renal insufficiency;
4. Liver function damage;
5. gestation;
6. receiving other immunosuppressants drug.


Age minimum: 15
Age maximum: 75
Gender: Both
Health Condition(s) or Problem(s) studied
IgA nephropathy
Intervention(s)
1:Kun-Xian Capsule;2:Leflunomide;
Primary Outcome(s)
the 24-hour urinary protein;albumin;creatinine;
Secondary Outcome(s)
ACR;Urine RBC;hemoglobin;
Secondary ID(s)
Source(s) of Monetary Support
Project funds
Secondary Sponsor(s)
Ethics review
Status: Approved
Approval date: 09/10/2018
Contact:
ZHU WENWEN
+86 028-83016039
Results
Results available:
Date Posted:
Date Completed:
URL:
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