- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04746196
Galectin-3 Level in Ankylosing Spondylitis Patients
Relationship Between Galectin-3 Level and Disease Activity in Ankylosing Spondylitis Patients
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Detailed histories of all participants were obtained, and systemic and rheumatologic examinations were performed. We excluded all participants who had a history of hyperlipidemia, liver, renal, hematological, familial thyroid, neoplastic, autoimmune infectious diseases and receiving anti-inflammatory drugs.
We measured serum galectin-3 levels using a commercial chemiluminescent microparticle immunoassay. The Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) was used to assess disease activity in AS patients.
Study Type
Enrollment (Actual)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Ankylosing spondylitis patients
- Healthy controls
Exclusion Criteria:
- Hyperlipidemia
- Liver diseases
- Renal diseases
- Hematological diseases
- Familial thyroid diseases
- Neoplastic diseases
- Autoimmune infectious diseases
- Receiving anti-inflammatory drugs.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
45 ankylosing spondylitis patients.
Patients diagnosed with ankylosing spondylitis according to Modified New York criteria were included in the study.
|
Serum galectin-3 concentration was measured using a commercial chemiluminescent microparticle immunoassay.
|
35 controls
Healthy controls
|
Serum galectin-3 concentration was measured using a commercial chemiluminescent microparticle immunoassay.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Relationship Between Galectin-3 Level and Disease Activity in Ankylosing Spondylitis Patients
Time Frame: 5 months
|
Correlation
|
5 months
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2016/85
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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