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RecruitingNCT07706569Updated Jul 15, 2026

Serum Fetuin-A and COMP Levels in Knee Osteoarthritis

An observational study in Knee Osteoarthritis and Osteoarthritis, Knee, sponsored by Antalya Training and Research Hospital. Recruiting at 1 site in Turkey (Türkiye). Per ClinicalTrials.gov, last updated 2026-07-15.

Sponsored by Antalya Training and Research Hospital · Observational

From the registry’s dates

  • Started Apr 2026; still recruiting 7 months later.
Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
180
Sex
All
01

Study summary

The purpose of this study is to investigate the relationship between the clinical and radiographic severity of knee osteoarthritis (OA) and the serum levels of specific biomarkers, namely Fetuin-A and Cartilage Oligomeric Matrix Protein (COMP). Osteoarthritis is a degenerative joint disease characterized by cartilage breakdown and low-grade inflammation. Investigating these biomarkers may help healthcare providers better understand the disease pathology, potentially leading to earlier diagnosis and improved tracking of disease progression. The study will compare two distinct groups: a patient group consisting of 120 individuals diagnosed with Grade 2-4 knee osteoarthritis, and a control group of 60 age- and sex-matched healthy volunteers with no history of joint disorders. Participants will undergo radiographic evaluations using the Kellgren-Lawrence classification system, alongside clinical and functional assessments, including pain severity scales, mobility metrics, and functional questionnaires. Fasting blood samples will be collected from all participants to measure serum Fetuin-A and COMP levels via laboratory analysis, and the Systemic Inflammation Response Index (SIRI) will be calculated. The collected data will be statistically analyzed to determine if biomarker levels significantly correlate with the severity of knee joint degeneration and functional impairment.

02

Conditions studied

  • Knee Osteoarthritis
  • Osteoarthritis, Knee

Keywords

  • Osteoarthritis, Knee
  • Fetuin-A
  • Cartilage Oligomeric Matrix Protein
  • Biological Biomarkers
  • Systemic Inflammation Response Index
  • Cross-Sectional Studies
03

In context

Osteoarthritis, Knee

3,292 studies on the registry are indexed under Osteoarthritis, Knee; 623 are open to participants now.

This study's planned enrollment of 180 is above the median of 100 across 486 observational studies indexed under Osteoarthritis, Knee.

Browse Osteoarthritis, Knee studies →

Lead sponsor

Antalya Training and Research Hospital is the lead sponsor of 104 studies on the registry; 12 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

The study population consisted of two main groups: a patient group and a healthy control group. The patient group included individuals who presented to the Physical Medicine and Rehabilitation Outpatient Clinics of SBÜ Antalya Training and Research Hospital and were diagnosed with primary knee osteoarthritis (Stage 2-4 according to the Kellgren-Lawrence classification system). The control group consisted of healthy volunteers of similar age and gender who did not have a known joint disorder, a history of knee pain, or a systemic inflammatory disease. All participants were selected using a single-center, hospital-based convenience sampling method during the specified study period.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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 .

Exclusion criteria

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 diseases. History of . Advanced renal or hepatic disease. Diagnosis of Diabetes Mellitus. Current use of systemic . Symptomatic osteoarthritis in other major joints (hip, hand, ankle, spine). Active systemic infection (fever ≥ 38, cough, diarrhea, dysuria, leukocytosis, or elevated CRP).
Terms in these criteria, in plain language(4)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
180 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • Knee Osteoarthritis Group

    120 patients diagnosed with primary knee osteoarthritis (Grade 2-4 according to Kellgren-Lawrence classification, 40 patients from each grade).

  • Healthy Control Group

    60 age- and sex-matched healthy volunteers without any knee pain, history of joint disease, or systemic inflammatory conditions.

06

What researchers measure

Primary outcomes

  1. Serum Fetuin-A Levels

    Measurement of serum Fetuin-A concentration using a human-specific ELISA kit to evaluate its relationship with radiographic and clinical severity.

    Time frame: Baseline (At the time of enrollment / single time point measurement)

Secondary outcomes

  1. Serum COMP (Cartilage Oligomeric Matrix Protein) Levels

    Time frame: Baseline

  2. Radiographic Severity via Kellgren-Lawrence (K-L) Classification

    Time frame: Baseline

  3. Clinical Severity and Functional Status via WOMAC Index

    Time frame: Baseline

  4. Systemic Inflammation Response Index (SIRI)

    (Neutrophil x Monocyte) / Lymphocyte

    Time frame: Baseline

  5. Pain Severity via Visual Analog Scale (VAS)

    Time frame: Baseline

  6. Functional Mobility via 10-Meter Walk Test (10MWT)

    Time frame: Baseline

  7. Lower Extremity Muscle Strength via 5-Times Sit-to-Stand Test (5x STS)

    Time frame: Baseline

07

Study locations

1 of 1 sites recruiting
  • S.B.U. Antalya Training and Research Hospital, Department of Physical Medicine and Rehabilitation
    Antalya, Turkey (Türkiye)
    Recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Apr 2026 (actual). Primary completion is estimated for Aug 2026, 4 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 11, 2026
First posted
Jul 15, 2026
StartActual
Apr 1, 2026
Primary completionEst.
Aug 30, 2026
CompletionEst.
Dec 30, 2026
Last update
Jul 15, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 15, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07706569
Responsible party
Burak Karaman (MD, Resident of Physical Medicine and Rehabilitation, Antalya Training and Research Hospital) — Principal investigator
First posted
Jul 15, 2026
Start date
Apr 1, 2026
Primary completion
Aug 30, 2026 (estimated)
Completion
Dec 30, 2026 (estimated)
Last update
Jul 15, 2026

Study contacts

Burak Karaman, MD
Contact
burak2498@gmail.com
+905079130762
Meral Bilgilisoy Filiz, Assoc. Prof.
Contact
mbilgilisoy@gmail.com
View the source record on ClinicalTrials.gov ↗

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