Value of Ultrasonographic Enthesitis Assessment in Spondyloarthritis | NCT04946539 | Trialant
CompletedObservationalUpdated Jul 1, 2021
Value of Ultrasonographic Enthesitis Assessment in Spondyloarthritis
ClinicalTrials.gov ID
NCT04946539
Lead Sponsor
Prof. Dr. Cemil Tascıoglu Education and Research Hospital OrganizationOTHER
Overall Status
Completed
Study Type
Observational
Enrollment
97Actual
Last Update Posted
Jul 1, 2021Actual
Start Date
Nov 2016Actual
Primary Completion Date
Jan 2017Actual
Completion Date
Mar 2017Actual
Brief Summary
The aim of the study is to determine how valuable ultrasonographic enthesitis to asssess disease activity, functionality and quality of life.
Spondyloarthritis
Enthesitis
Ultrasonography
Ages Eligible for Study
Adult (18-64)
Sexes Eligible for Study
All
Accepts Healthy Volunteers
No data available
Eligibility Criteria
Inclusion Criteria:
Spondyloarthritis patients that fulfill 2009 ASAS criteria
Exclusion Criteria:
history of elbow, ankle or knee surgery, local injection at the examination sites within the six weeks, peripheral neuropathy, infection and wound at examination site
Observational Model
Case-Control
Time Perspective
Cross-Sectional
No central contacts
There are no central contacts for this study.
No locations
There are no locations for this study.
Lead Sponsor
Prof. Dr. Cemil Tascıoglu Education and Research Hospital OrganizationOTHER