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Active Not RecruitingNCT07439107

Treatment Outcomes for Osteochondritis Dissecans of the Knee: A Cohort Study

An Ambidirectional Cohort Study on Treatment Strategies for Osteochondritis Dissecans of the Knee

Status
Active Not Recruiting
Phase
Study type
Observational
Enrollment
254 (estimated)
Sponsor
Peking University Third Hospital · Academic / Other
Sex
All
Age
6 Years – 40 Years
Healthy volunteers
Not accepted

Summary

This is a non-randomized, observational, ambidirectional cohort study. Approximately 254 participants with knee OCD will be recruited from Peking University Third Hospital, China, comprising a prospective cohort (n=177) and a retrospective cohort (n=77). The study aims to observe and compare the long-term outcomes among patients receiving different standard-of-care treatments. Treatment decisions (conservative management or specific surgical interventions) are made by clinicians and patients according to prevailing clinical guidelines and individual conditions, independent of this study. Based on the treatment they receive in clinical practice, participants will be categorized into two main exposure groups: the conservative treatment group and the surgical treatment group. The surgical group will be further stratified into six subgroups according to the specific surgical technique employed. All participants will enter a follow-up phase lasting up to 24 months. Assessments will include the Magnetic Resonance Observation of Cartilage Repair Tissue (MOCART) score (primary outcome), the International Knee Documentation Committee (IKDC) Subjective Knee Form, pain intensity (Visual Analog Scale, VAS), Lysholm knee score, as well as the incidence of complications and Adverse Events (AEs)/Serious Adverse Events (SAEs). For patients undergoing surgery, these measurements will be conducted at the following time points: preoperatively, intraoperatively, and postoperatively at 7 days, 3 months, 6 months, 12 months, and 24 months. For patients under conservative management, follow-up assessments will be conducted at corresponding clinical time points.

Conditions

Interventions

TypeNameDescription
OTHERClinical Management for OCD (Observed)This is not an intervention assigned by the study. It encompasses the spectrum of standard conservative and surgical treatments that participants may receive as part of independent clinical care. The specific treatment each participant receives is documented and used to define the study cohorts for observational comparison.

Timeline

Start date
2026-01-01
Primary completion
2028-12-31
Completion
2028-12-31
First posted
2026-02-27
Last updated
2026-02-27

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07439107. Inclusion in this directory is not an endorsement.