Clinical Registry Assessment of the Missouri Osteochondral Allograft Preservation System - MOPS
Enrolling by invitation
Conditions studied: Symptomatic Osteochondral Defect(s), Cartilage, Meniscus, Ankle, Knee, Shoulder, Hip
In brief
With institutional review board approval and informed consent, patients are prospectively enrolled into a registry to follow outcomes after osteochondral allograft (OCA) and/or meniscal allograft transplantation. Patients are included when 1 year followup data are available, including complications and reoperations, patient reported outcome measures (PROMs), compliance with rehabilitation, revisions, and failures. In addition, MOPS grafts are compared to standard preservation grafts, and unipolar, multisurface, and bipolar cohorts, as well as patient compliance variables, are compared.
Key facts
- Study ID
- NCT02503228
- Run by
- University of Missouri-Columbia
- People needed
- 5000
- Starts
- 2015-06-01
- Expected to finish
- 2050-12-01
- Last updated by the study team
- 2026-07-30
Who can join
Age: 13 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adults and children age ≥13 years
- Knee, hip, ankle, or shoulder osteochondral defect ≥15mm as determined by MRI or diagnostic knee arthroscopy for allograft transplantation
- Must be physically and mentally willing and able to comply with postoperative and routinely scheduled clinical and radiographic evaluations.
- Must be able to read and understand English or a language for which translated versions of the patient reported questionnaires and Informed consent form are available.
- Must be able to sign informed consent and must voluntarily sign the Institutional Review Board (IRB)/Independent Ethics Committee (IEC)-approved subject Informed Consent Form.
You may not qualify if…
- Is a prisoner
- Is receiving workman's compensation
- Subject is mentally incompetent such that would preclude the subject from providing adequate consent and/or complying with study requirements
Where it is running
- University of Missouri — Columbia, Missouri, United States
Full record on ClinicalTrials.gov
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