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Ankylosing Spondylitis and Spondyloarthritis Evaluation Tool Study

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01302730
Recruitment Status : Completed
First Posted : February 24, 2011
Last Update Posted : November 8, 2013
Sponsor:
Collaborators:
University of California, San Francisco
Oregon Health and Science University
Cedars-Sinai Medical Center
Information provided by (Responsible Party):
Eswar Krishnan, Stanford University

Tracking Information
First Submitted Date February 22, 2011
First Posted Date February 24, 2011
Last Update Posted Date November 8, 2013
Study Start Date April 2011
Actual Primary Completion Date March 2012   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures
 (submitted: November 6, 2013)
Physician diagnosis of Ankylosing Spondylitis [ Time Frame: 6 months ]
Original Primary Outcome Measures Not Provided
Change History
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title Ankylosing Spondylitis and Spondyloarthritis Evaluation Tool Study
Official Title A Self-Administered Questionnaire for Early Detection of Axial Spondyloarthritis
Brief Summary This study aims to test whether a new instrument (questionnaire) is useful for identifying patients with ankylosing spondylitis.
Detailed Description Not Provided
Study Type Observational
Study Design Time Perspective: Prospective
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Non-Probability Sample
Study Population All patients referred to rheumatologist office will be potentially eligible.
Condition
  • Ankylosing Spondylitis
  • Spondylarthritis
Intervention Not Provided
Study Groups/Cohorts Not Provided
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Completed
Actual Enrollment
 (submitted: November 6, 2013)
490
Original Estimated Enrollment
 (submitted: February 23, 2011)
400
Actual Study Completion Date November 2013
Actual Primary Completion Date March 2012   (Final data collection date for primary outcome measure)
Eligibility Criteria

Inclusion Criteria:

  • Ability to provide informed consent

Exclusion Criteria:

  • Inability to provide informed consent
Sex/Gender
Sexes Eligible for Study: All
Ages 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers No
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries United States
Removed Location Countries  
 
Administrative Information
NCT Number NCT01302730
Other Study ID Numbers STANIRB-20278
Has Data Monitoring Committee No
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement Not Provided
Responsible Party Eswar Krishnan, Stanford University
Study Sponsor Stanford University
Collaborators
  • University of California, San Francisco
  • Oregon Health and Science University
  • Cedars-Sinai Medical Center
Investigators
Principal Investigator: Eswar Krishnan Stanford University
PRS Account Stanford University
Verification Date November 2013