RecruitingNCT07293949

Ultrasonographic Evaluation of Talar Cartilage Thickness in Patients With Spinal Cord Injury

Ultrasonographic Evaluation of Talar Cartilage Thickness in Patients With Spinal Cord Injury: A Cross-Sectional Case-Control Study


Sponsor

Gaziosmanpasa Research and Education Hospital

Enrollment

76 participants

Start Date

Dec 20, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

Spinal cord injury patients often present with musculoskeletal comorbidities, including osteoarthritis. Early detection of cartilage damage is important for preventing osteoarthritis progression. This study aims to compare the talar cartilage thicknesses of spinal cord injury patients with healthy subjects. The secondary aim is to investigate a correlation between the talar cartilage thickness and disease-related parameters. The patient group is to be assessed for talar cartilage thickness (via ultrasound), functional status, spasticity, and ambulation levels.


Eligibility

Min Age: 18 YearsMax Age: 60 Years

Inclusion Criteria6

  • 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 Criteria7

  • 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

Interested in this trial?

Get notified about updates and connect with the research team.


Locations(1)

Gaziosmanpasa Training and Research Hospital

Istanbul, Turkey (Türkiye)

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07293949


Related Trials