Serum Fetuin‑A and COMP levels in knee osteoarthritis
Official title: The Relationship Between Clinical and Radiographic Severity of Knee Osteoarthritis and Serum Fetuin-A and COMP Levels: A Controlled Cross-Sectional Study
Run by Antalya Training and Research Hospital · NCT07706569 · Data updated 2026-11-12
This study tests whether levels of Fetuin‑A and COMP in the blood relate to how severe knee osteoarthritis is in patients compared with healthy volunteers.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 180 (estimated) |
| Sponsor | Antalya Training and Research Hospital Government |
| Locations | 1 site (Antalya) |
| Status | Recruiting |
| Started | April 1, 2026 |
| Main results expected | August 30, 2026 |
| Study ends | December 30, 2026 |
| Registry record updated | July 15, 2026 |
| Trial ID | NCT07706569 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with knee osteoarthritis who meet ACR criteria and are graded 2–4 on the Kellgren‑Lawrence scale.
✕Probably not a fit
Individuals without knee OA or with non‑knee inflammatory conditions may not benefit from this biomarker analysis.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study compares serum biomarkers Fetuin‑A and COMP with clinical and radiographic severity of knee osteoarthritis. A total of 180 participants include 120 patients with Kellgren‑Lawrence grade 2–4 OA and 60 age‑ and sex‑matched healthy controls. Participants will undergo radiographs, clinical and functional assessments, and biomarker measurements to explore associations between biomarker levels and disease severity. The goal is to see if these biomarkers help reflect disease state and progression. Interventions are not used; the study is observational in design.
Why it matters
Potential benefit: If successful, Fetuin‑A and COMP could become part of a blood test to help assess OA severity and monitor progression.
How similar studies have gone: Previous research has shown associations between these biomarkers and OA features, but the utility for routine clinical assessment remains under investigation.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: \- Diagnosis of knee osteoarthritis according to ACR (American College of Rheumatology) criteria. Knee osteoarthritis classified as Grade 2, 3, or 4 according to Kellgren-Lawrence (K-L) grading. Volunteering to participate and providing signed informed consent. Exclusion Criteria: * Secondary post-traumatic knee osteoarthritis, history of major knee injury or joint infection. Signs of acute joint inflammation (swelling, heat increase, erythema). History of knee surgery (open or arthroscopic). Systemic inflammatory or autoimmune diseases. History of malignancy. Advanced renal or hepatic disease. Diagnosis of Diabetes Mellitus. Current use of systemic corticosteroids. Symptomatic osteoarthritis in other major joints (hip, hand, ankle, spine). Active systemic infection (fever ≥ 38, cough, diarrhea, dysuria, leukocytosis, or elevated CRP).
Where it's running
-
S.B.U. Antalya Training and Research Hospital, Department of Physical Medicine and Rehabilitation
Antalya, Turkey (Türkiye) Recruiting
Study contacts
- Study coordinator: Burak Karaman, MD
- Email: burak2498@gmail.com
- Phone: +905079130762
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.