Ankylosing Spondylitis and Spondyloarthritis Evaluation Tool Study
Completed
- Conditions
- Ankylosing SpondylitisSpondylarthritis
- Registration Number
- NCT01302730
- Lead Sponsor
- Stanford University
- Brief Summary
This study aims to test whether a new instrument (questionnaire) is useful for identifying patients with ankylosing spondylitis.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 490
Inclusion Criteria
- Ability to provide informed consent
Exclusion Criteria
- Inability to provide informed consent
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Physician diagnosis of Ankylosing Spondylitis 6 months
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie axial spondyloarthritis in NCT01302730 observational study?
How does the self-administered questionnaire in NCT01302730 compare to standard diagnostic tools for ankylosing spondylitis?
What biomarkers are associated with early detection of axial spondyloarthritis in Stanford University's NCT01302730 study?
What adverse events are reported in axial spondyloarthritis screening tools like NCT01302730's questionnaire?
What are the potential therapeutic targets identified in NCT01302730 for spondyloarthritis management?
Trial Locations
- Locations (1)
Stanford University
🇺🇸Stanford, California, United States
Stanford University🇺🇸Stanford, California, United States