Osteochondritis Dissecans of Knee Prospective Cohort

Summary

The Cohort is a multi-site prospective data collection study that will enroll any patient with diagnosis of knee OCD (confirmed by a standard of care x-ray or MRI). Patients will be followed for up to the next 50 years of their lives to study courses of care, disease progression, treatment/surgical options/results, and specific sports-related outcomes in athletic patients. Subjects will complete quality of life surveys as part of the Cohort. Course of care will not be affected.

Conditions

• Osteochondritis Dissecans

Interventions

OTHER

Other: observational only- no intervention

Other: observational only- no intervention

Sponsors & Collaborators

• Altona Children's Hospital

  collaborator OTHER

• Boston Children's Hospital

  collaborator OTHER

• Children's Hospital Medical Center, Cincinnati

  collaborator OTHER

• Children's Health Andrews Institute for Orthopaedics & Sports Medicine

  collaborator UNKNOWN

• Children's Healthcare of Atlanta

  collaborator OTHER

• Children's Hospital Colorado

  collaborator OTHER

• Children's Hospital of Philadelphia

  collaborator OTHER

• Children's Hospital and Health System Foundation, Wisconsin

  collaborator OTHER

• Children's Mercy Hospital Kansas City

  collaborator OTHER

• Connecticut Children's Medical Center

  collaborator OTHER

• Hospital for Special Surgery, New York

  collaborator OTHER

• Kaiser Permanente

  collaborator OTHER

• Mayo Clinic

  collaborator OTHER

• National University Hospital, Singapore

  collaborator OTHER

• Rady Children's Hospital, San Diego

  collaborator OTHER

• Stanford University

  collaborator OTHER

• Tennessee Orthopedic Alliance

  collaborator OTHER

• Texas Scottish Rite Hospital for Children

  collaborator OTHER

• The Rocky Mountain Hospital for Children

  collaborator UNKNOWN

• The Hospital for Sick Children

  collaborator OTHER

• Göteborg University

  collaborator OTHER

• University of Minnesota/TRIA Orthopaedic Center

  collaborator UNKNOWN

• Washington University School of Medicine

  collaborator OTHER

• University of Pennsylvania

  lead OTHER

Principal Investigators

• James L Carey, MD · University of Pennsylvania

Eligibility

Sex

ALL

Healthy Volunteers

No

Timeline & Regulatory

Start

2014-05-31

Primary Completion

2064-05-31

Completion

2064-12-31

Countries

• United States

Study Locations