Osteochondritis Dissecans Clinical Trial
Official title:
Examination and Post-operative Rehabilitation of University Athletes With Osteochondral Lesions of the Knee: A Case Series Report
NCT number | NCT03452098 |
Other study ID # | IRB-FY18-11 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | January 2011 |
Est. completion date | November 2018 |
Verified date | February 2019 |
Source | California State University, Northridge |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
A case-series review was performed on five collegiate athletes with osteochondral lesions of the knee at California State University, Northridge (CSUN). All subjects received surgical intervention to treat the defect. The surgeries performed were either an Osteoarticular Transfer System (OATS) procedure and/or a Microfracturing procedure. Subjects were treated post-operatively by the CSUN team physical therapist and/or athletic trainers at CSUN. This paper seeks to provide information about osteochondral defects of the knee, the surgical interventions, and a protocol for post-operative treatment and rehabilitation of such injuries.
Status | Completed |
Enrollment | 5 |
Est. completion date | November 2018 |
Est. primary completion date | November 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Student athlete at CSUN - Diagnosed with Osteochondral dissecans (OCD) - Underwent surgical procedure to treat OCD - Treated postoperatively by the team physical therapist and/or athletic trainers at CSUN. Exclusion Criteria: - No concurrent ligamentous injures to the knee during the time of subject participation in the study |
Country | Name | City | State |
---|---|---|---|
United States | California State University, Northridge | Northridge | California |
Lead Sponsor | Collaborator |
---|---|
California State University, Northridge |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Level of Function | Determined by subject's ability to return to play of his/her respective sport | Through study completion; an average of 6 months | |
Secondary | Pain | Pain as measured by the Visual Analog Scale (VAS), 0 (No pain) - 10 (Severe Pain) | Monthly until the completion of the study; an average of 6 months |
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