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Clinical Trial Details — Status: Completed

Administrative data

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

Study information

Verified date February 2019
Source California State University, Northridge
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

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

Study Design


Locations

Country Name City State
United States California State University, Northridge Northridge California

Sponsors (1)

Lead Sponsor Collaborator
California State University, Northridge

Country where clinical trial is conducted

United States, 

Outcome

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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