Actively Recruiting

Age: 18Years - 50Years
All Genders
ID04536103

Multi-Vendor Multi-Site Novel Accelerated MRI Relaxometry for Early Detection of Cartilage Degeneration in Osteoarthritis

Led by Xiaojuan Li · Updated on 2026-02-27

88

Participants Needed

1

Research Sites

43 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating advanced MRI imaging techniques to improve early detection and assessment of cartilage health in people at risk for osteoarthritis (OA). Current diagnosis relies on X-rays and clinical signs that detect late-stage OA, so this study focuses on developing faster, more reliable MRI methods using T1c1 and T2 relaxation times. These imaging biomarkers may help identify early cartilage degeneration and disease progression, addressing a critical need for better tools in clinical trials and patient care. The study will develop and test novel accelerated MRI methods to reduce imaging time while maintaining accuracy. It involves creating calibration phantoms and standardizing protocols across MRI systems from multiple vendors (Siemens, GE, Philips). The research includes four groups: healthy volunteers for technique evaluation, traveling volunteers scanned at multiple sites for cross-validation, patients with acute ACL tears to study early OA changes, and matched controls. Scans will be performed at baseline and after one year to compare standard and accelerated imaging methods. Participants will undergo MRI scans using the new and standard techniques to measure cartilage health and degeneration. The study assesses site and vendor reproducibility and tracks changes in patients with ACL injuries. Outcomes include knee MRI results over several years, with detailed analysis of imaging consistency and cartilage condition. The total study duration for participants varies by group, with some scanned multiple times over up to five years to monitor cartilage changes and validate the imaging approach.

CONDITIONS

Brief Title

Multi-Vendor Multi-Site Novel Accelerated MRI Relaxometry

Who Can Participate

Age: 18Years - 50Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Group 1: Age over 18 years
  • Group 2: Age 18 to 50 years
  • Group 3: Age 18 to 50 years; acute full ACL tear in one knee; uninjured contralateral knee; scheduled for ACL reconstruction and standard rehabilitation
  • Group 4: Age 18 to 50 years
Not Eligible

You will not qualify if you...

  • Group 1: Contraindications to MRI such as severe claustrophobia or implanted devices like neurostimulators, pacemakers, aneurysm clips; pregnancy
  • Group 2: Contraindications to MRI as above; pregnancy; history of osteoarthritis or inflammatory arthritis; previous injury or surgery on either knee
  • Group 3: Contraindications to MRI as above; pregnancy; inability to undergo standard pre- and post-injury/operative rehabilitation
  • Group 4: Contraindications to MRI as above; pregnancy; history of osteoarthritis or inflammatory arthritis; previous injury or surgery on either knee

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Baseline and 1-year assessments

Participants undergo MRI scans using standard and accelerated T1ρ and T2 protocols to evaluate cartilage and knee health.

2 visits (in-person) at baseline and 1-year

Long-term Monitoring

Duration - Up to 1 year

Participants are observed over time to assess changes in cartilage degeneration and knee health using advanced MRI techniques.

Follow-up visit at 1 year (in-person)

Trial Site Locations

Total: 1 location

1

Cleveland Clinic Foundation

Cleveland, Ohio, United States, 44195

Actively Recruiting

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Research Team

X

Xiaojuan Li, PhD

J

Jennifer Baldwin

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

4

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