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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT04660955
Other study ID # 19-573
Secondary ID R01AR075422
Status Enrolling by invitation
Phase
First received
Last updated
Start date January 1, 2020
Est. completion date January 1, 2030

Study information

Verified date February 2024
Source The Cleveland Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In this study, a total of 219 subjects from the MOON nested cohort will be studied at CCF, Vanderbilt and OSU, Table 1. Among them, some will have added MRI during their 10-year visit for the MOON study. Some subjects who finished their 10-year visit for the MOON Onsite study already will be called back to have MRI. PROMs and other information of these subjects will be collected through the MOON study.


Description:

In this study, a total of 219 subjects from the MOON nested cohort will be studied at CCF, Vanderbilt and OSU, Table 1. Among them, some will have added MRI during their 10-year visit for the MOON study. Some subjects who finished their 10-year visit for the MOON Onsite study already will be called back to have MRI. PROMs and other information of these subjects will be collected through the MOON study. In addition, 30 age-, sex- and BMI-matched control subjects (10 from each site) will be recruited and scanned for MRI. PROMs (KOOS, IKDC, Marx, SF-36) will be collected from these controls. Among the 10 controls recruited locally at CCF, five will also travel to OSU and Vanderbilt to be scanned at the other two sites for cross-validation among the three sites. There will be a separate consent for the 5 controls that will be traveling to each of the 3 sites for the scans. The remaining 25 controls will be tested at only their local site.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 219
Est. completion date January 1, 2030
Est. primary completion date January 1, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 22 Years to 45 Years
Eligibility Inclusion Criteria: - Enrolled in MOON Onsite Study - 12-33 years old at baseline (22-45 years for this study); - ACL tear during a sport; no previous knee injury; - No graft rupture during follow-up; - No history of surgery on the contralateral knee; - No MRI contraindications Exclusion Criteria: - History of surgery on contralateral knee - Afraid of enclosed spaces

Study Design


Related Conditions & MeSH terms


Intervention

Other:
No Intervention - Observational study with MRI
90 minute MRI of the knees

Locations

Country Name City State
United States Cleveland Clinic Cleveland Ohio

Sponsors (4)

Lead Sponsor Collaborator
The Cleveland Clinic National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), Ohio State University, Vanderbilt University Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cartilage health status Quantitative MRI will be used to quantify cartilage health. Specifically, cartilage MR T1rho and T2 relaxation times will be quantified for cartilage of the knee that had ACL reconstruction, and compared to the contralateral uninjured knee. At 10-years after ACL reconstruction
Secondary Patient reported outcomes Pain score (0-100) evaluated using Knee injury and Osteoarthritis Outcome Score (KOOS) At 10-years after ACL reconstruction
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