Can ultrasound spot early arthritis risk in spinal injury patients?
NCT ID NCT07293949
First seen Jun 24, 2026 · Last updated Jul 29, 2026 · Updated 4 times
Summary
This study uses ultrasound to measure the thickness of ankle cartilage in people with spinal cord injuries and compares it to healthy individuals. The goal is to see if cartilage damage starts early, which could help prevent osteoarthritis. Researchers will also assess participants' mobility and muscle stiffness. The study is currently recruiting 76 adults aged 18 to 60.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could help doctors identify early cartilage damage in spinal cord injury patients, potentially leading to better prevention of osteoarthritis.
- What could go wrong
- This is an observational study, not a treatment trial. It only measures cartilage thickness and does not test any intervention, so it cannot directly improve health outcomes.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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76 people
The number who actually took part.
- Started
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Dec 2025
- Finished
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Jun 2026
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Thirty-eight SCI patients who apply to Physical Medicine and Rehabilitation outpatient and inpatient clinic between November 2025-January 2026 will be included in the study. Thirty-eight age, gender, and BMI-matched healthy participants who are literate, give oral and written consent without any additional disease will be formed as the control group.
- Ages
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18 to 60 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Aged between 18 to 60 years, * Cervical, thoracal or lumber level of spinal cord injury * AIS (American Spinal Injury Association Impairment Scale) Level A, B, C, or D * Assisted ambulation of any kind * Literacy * Giving oral and written consent to participate in the study Exclusion Criteria: * Patients with sacral level injury * AIS E * MAS 4 level of spasticity * History of any lower extremity operation * History of fracture * Botulinum toxin injection in the last 6 months * Existing diagnosis of any rheumatologic or endocrine diseases
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Gaziosmanpasa Training and Research Hospital
Istanbul, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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