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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: 11 December 2017
Main ID:  ChiCTR-INR-17013574
Date of registration: 2017-11-28
Prospective Registration: Yes
Primary sponsor: The First Affiliated Hospital of Heilongjiang Chinese Medicine Colledge
Public title: Clinical Study on Treating Ankylosing Spondylitis with Chinese Herbal Decoction Zhitongzhu Decoction
Scientific title: Clinical Study on Treating Ankylosing Spondylitis with Chinese Herbal Decoction Zhitongzhu Decoction
Date of first enrolment: 2018-06-01
Target sample size: control group :40; Intervention group :40;
Recruitment status: Pending
URL:  http://www.chictr.org.cn/showproj.aspx?proj=22959
Study type:  Interventional study
Study design:  Randomized parallel controlled trial  
Phase:  New Treatment Measure Clinical Study
Countries of recruitment
China
Contacts
Name: Ying Tong   
Address:  26 Heping Road, Xiangfang District, Harbin, Heilongjiang, China
Telephone: +86 186867800398
Email: tymm0451@126.com
Affiliation:  The First Affiliated Hospital of Heilongjiang Chinese Medicine Colledge
Name: Zhang Weiping   
Address:  26 Heping Road, Xiangfang District, Harbin, Heilongjiang, China
Telephone: +86 18246078873
Email: 1365175867@qq.com
Affiliation:  The First Affiliated Hospital of Heilongjiang Chinese Medicine Colledge
Key inclusion & exclusion criteria
Inclusion criteria: Forty patients diagnosed according to the International Classification of Ankylosing Spondylitis were all outpatients and inpatients with rheumatism and immunology in our hospital. Choices:
(1) male patients, aged 16 to 25 years old;
(2) did not use corticosteroids, HCQs and other drugs within 1 month before enrollment.

Exclusion criteria: (1) allergic constitution;
(2) accompanied by viral hepatitis, alcoholic liver disease, fatty liver and drug-induced liver disease.


Age minimum: 16
Age maximum: 25
Gender: Male
Health Condition(s) or Problem(s) studied
Ankylosing spondylitis
Intervention(s)
control group :Leflunomide; Intervention group :Chinese herbalshentongzhuyudecoction;
Primary Outcome(s)
Rheumatoid factor;HL-B27;
Secondary Outcome(s)
Secondary ID(s)
Source(s) of Monetary Support
Self sponsored and department sponsored
Secondary Sponsor(s)
Ethics review
Status: Not approved
Approval date: 26/08/2013
Contact:
Results
Results available:
Date Posted:
Date Completed:
URL:
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