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RecruitingBone Diseases, InfectiousMusculoskeletal DiseasesJoint Diseases

Multi-Vendor Multi-Site Novel Accelerated MRI Relaxometry

Eligible age

18–50 yrs

Accepts

All genders

Locations

1 state

Healthy volunteers

No

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About this study

Currently the diagnosis of OA is based on radiographs and clinical findings, which is limited to detecting late-stage disease. There is a pressing, unmet clinical need for robust assessment of early changes in cartilage health. Towards this goal, extensive efforts are ongoing to develop quantitative MRI for cartilage matrix analysis. MR T1ρ and T2 relaxation times have shown to be promising imaging biomarkers for early cartilage degeneration and prediction of disease progression. However, many challenges remain to clinically applying these techniques, including lack of standardized acquisition and quantification methods, and long acquisition times. The study aims to develop novel, fast and reproducible MR T1ρ and T2 relaxation time imaging methods on MR systems from multiple vendors and establish a platform for standardization and cross validation of these measures as a tool for clinical trials using such techniques. Following method validation, patients at risk for osteoarthritis will be tested.

Sponsor: Xiaojuan Li

You may qualify if…

  • Group 1
  • 1\. Age \> 18
  • Group 2
  • 1\. Age 18-50
  • Group 3
  • 1. Age 18-50
  • 2. Sustain an acute full ACL tear in one knee; the contralateral knee uninjured
  • 3. Undergo ACL reconstructions and standard rehabilitation

You may not qualify if…

  • Group 1
  • 1. Contraindication to MRI such as severe claustrophobia and implanted devices such as neurostimulators, pacemakers, aneurysm clips etc.
  • 2. Pregnancy.
  • Group 2
  • 1. Contraindication to MRI such as severe claustrophobia and implanted devices such as neurostimulators, pacemakers, aneurysm clips etc.
  • 2. Pregnancy.
  • 3. History of osteoarthritis and inflammatory arthritis
  • 4. Previous injury and/or surgery on either knee

Where it's recruiting

Ohio

Cleveland

Source: ClinicalTrials.gov · NCT04536103 · last updated 2026-02-27