The purpose of this registry is to create the first centralized, comprehensive database of knee OCD cases to act as a platform for future studies on OCD, providing ROCK institutions with a large database including the different types of OCD lesions and variables associated with the disease characteristics, course of treatment and healing, and long term follow up. Projects stemming from analysis of information collected in the registry will help develop better understanding of the disease and its causes, progression, and the best treatment patients with OCD can receive based on their history and lesion characteristics.
PC Essential Study Documents:
Manual of Operations v. 5.0 | Tracked Version
Informed Consent | Tracked Version
Child Assent | Tracked Version
PC Case Report Forms:
Form 1: Screening and Eligibility
Form 2A: Baseline Questionnaire – Adult
Form 2B: Baseline Questionnaire – Child
Form 2C: Baseline Questionnaire – Surgeon
REDCap Database:
Study Updates:
2018, February (Annual Meeting)
2017, January (Annual Meeting)