Skip to content

Osteochondritis Dissecans of Knee Prospective Cohort

ROCK Comprehensive Prospective Cohort for Osteochondritis Dissecans of the Knee

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02771496
Enrollment
3000
Registered
2016-05-13
Start date
2014-05-01
Completion date
2074-12-01
Last updated
2026-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteochondritis Dissecans

Brief 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.

Detailed description

Patients will be recruited and consented at the visit in which their eligibility is determined. Once a patient is eligible and provides informed consent, he or she will be in the study for up to 50 years, or until his or her OCD lesion is healed successfully. At the initial visit, a subject will complete a basic medical history form, and three questionnaires: the IKDC Subjective questionnaire (ages over 18) or the PEDI-IKDC Subjective questionnaire (ages under 18); the KOOS questionnaire; and the Marx Activity Scale (adult) or Pedi-FABS Scale (pediatric). Patients will then continue with their normal course of care as determined by their surgeon and care team. Mandatory surveys (same as above) will be collected from patients at 2 years, 5 years, 10 years, and 25 years. Patients who cannot return to clinic will have the option to complete the assessments and return in pre-stamped and addressed return envelopes provided by the clinical site the subject is a patient at. Any other follow-up visits between these time intervals will also be options for patients to complete these assessments, however patients will not complete them any closer than intervals 12 weeks apart in order to prevent redundancy. Additionally, at the initial visit, the surgeon will complete a routine patient history and physical exam, which will be collected. Any surgical procedures or physical therapy a patient undergoes for treatment of his or her OCD lesion will also be documented and collected. At follow-up visits, surgeons will complete their own physical exam follow-up assessment forms, which will be collected.

Interventions

OTHEROther: observational only- no intervention

Other: observational only- no intervention

Sponsors

University of Pennsylvania
Lead SponsorOTHER
Altona Children's Hospital
CollaboratorOTHER
Boston Children's Hospital
CollaboratorOTHER
Children's Hospital Medical Center, Cincinnati
CollaboratorOTHER
Children's Health Andrews Institute for Orthopaedics & Sports Medicine
CollaboratorUNKNOWN
Children's Healthcare of Atlanta
CollaboratorOTHER
Children's Hospital Colorado
CollaboratorOTHER
Children's Hospital of Philadelphia
CollaboratorOTHER
Children's Hospital and Health System Foundation, Wisconsin
CollaboratorOTHER
Children's Mercy Hospital Kansas City
CollaboratorOTHER
Connecticut Children's Medical Center
CollaboratorOTHER
Hospital for Special Surgery, New York
CollaboratorOTHER
Kaiser Permanente
CollaboratorOTHER
Mayo Clinic
CollaboratorOTHER
National University Hospital, Singapore
CollaboratorOTHER
Rady Children's Hospital, San Diego
CollaboratorOTHER
Stanford University
CollaboratorOTHER
Tennessee Orthopedic Alliance
CollaboratorOTHER
Texas Scottish Rite Hospital for Children
CollaboratorOTHER
The Rocky Mountain Hospital for Children
CollaboratorUNKNOWN
The Hospital for Sick Children
CollaboratorOTHER
Göteborg University
CollaboratorOTHER
University of Minnesota/TRIA Orthopaedic Center
CollaboratorUNKNOWN
Washington University School of Medicine
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Diagnosis of osteochondritis dissecans or focal articular cartilage defects as confirmed by x-ray or MRI

Exclusion criteria

* Non-confirmed diagnosis (i.e. patient does not yet have imaging confirmation)

Design outcomes

Primary

MeasureTime frameDescription
IKDC questionnairebaseline up to 50 yearsThe primary outcome endpoint for this study is the patient's score on the IKDC Subjective questionnaire, or PEDI-IKDC Subjective questionnaire for patients under 18 years of age.
PEDI-IKDC questionnairebaseline up to 50 yearsThe primary outcome endpoint for this study is the patient's score on the IKDC Subjective questionnaire, or PEDI-IKDC Subjective questionnaire for patients under 18 years of age.

Secondary

MeasureTime frameDescription
KOOS Knee scorebaseline up to 50 yearsThe Knee injury and Osteoarthritis Outcome Score (KOOS) evaluates short-term and long-term symptoms and function in subjects with knee injury and osteoarthritis.
Marx Activity Score questionnairebaseline up to 50 yearsMeasure of physical activity at healthiest and most active state from time of taking to year prior.
Pedi-FABS Scorebaseline up to 50 yearsAn eight-item scale that measures level of physical activity and fitness.
Radiographic Healingbaseline up to 50 yearsVisualization of bone healing through x-ray images.

Countries

United States

Contacts

CONTACTMounika Ponakala, MS
mounika.ponakala@pennmedicine.upenn.edu6093343767
PRINCIPAL_INVESTIGATORJames L Carey, MD

University of Pennsylvania

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 28, 2026