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Clinical Registry Assessment of the Missouri Osteochondral Allograft Preservation System - MOPS

NCT02503228 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 5000

Last updated 2025-07-15

No results posted yet for this study

Summary

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.

Conditions

  • Symptomatic Osteochondral Defect(s)
  • Cartilage, Meniscus, Ankle, Knee, Shoulder, Hip

Interventions

PROCEDURE

Standard of care osteochondral and or meniscal allograft transplantation

Standard of care osteochondral and or meniscal allograft transplantation

Sponsors & Collaborators

  • University of Missouri-Columbia

    lead OTHER

Eligibility

Min Age
13 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-30
Primary Completion
2050-12-31
Completion
2050-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02503228 on ClinicalTrials.gov