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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: 18 April 2017
Main ID:  ChiCTR-ONRC-11001846
Date of registration: 2011-12-28
Prospective Registration: No
Primary sponsor: Department of Clinical Immunology, Xijing Hospital, Fourth Military Medical University
Public title: The research of immue state and current treatment in Ankylosing spondylitis
Scientific title: The research of immue state and current treatment in Ankylosing spondylitis
Date of first enrolment: 2009-12-03
Target sample size: Traditional therapy group:500;biological agent group:500;thalidomide group:500;
Recruitment status: Completed
URL:  http://www.chictr.org.cn/showproj.aspx?proj=7701
Study type:  Observational study
Study design:  Non randomized control  
Phase:  Pilot study
Countries of recruitment
Contacts
Name: Ping Zhu   
Address:  15 West Changle Road, Xi'an, Shaanxi, China
Telephone: +86 029 84771581
Email: zhuping@fmmu.edu.cn
Affiliation: 
Name: Qing Han   
Address:  15 West Changle Road, Xi'an, Shaanxi, China 710032
Telephone: +86 13572821171
Email: 13572821171@139.com
Affiliation:  Department of Clinical Immunology, Xijing Hospital,Fouth MilitaryMedical University
Key inclusion & exclusion criteria
Inclusion criteria: 1. patients hadto meet the modified New York clinical criteria in 1984 for definite Ankylosing spondylitis;
2. patients can provid the informed consent document in writting, and agree to abide by the requirement for the research plan.

Exclusion criteria: 1. Female patients who are pregnant or breastfeeding;
2. patients who have severe systemic diaease; no perceptibility or can not take care of onself in daily life;malignant tumor.


Age minimum: 18
Age maximum: 65
Gender: Both
Health Condition(s) or Problem(s) studied
Ankylosing spondylitis
Intervention(s)
Traditional therapy group:DMARDs;biological agent group:biological agent;thalidomide group:thalidomide;
Primary Outcome(s)
TH1 cell quantity;Treg cell quantity;TH17 cell quantity;the level of associated cytokine;expression of assocoated Transcription factors;ASDAS;BASDAI;BASFI;BASMI;Harris score;radiology;magnetic resonance imaging;CRP;ESR;
Secondary Outcome(s)
Secondary ID(s)
Source(s) of Monetary Support
Xijing Hospital, Fourth Military Medical University
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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