Retrospective, multi-center, chart review (only to include data that is part of the surgeons' standard practice)
The purpose of this study is to leverage standard of care data to provide further characterization of clinical outcomes following shoulder, hip and knee joint surgeries. * Primary Objective: To describe clinical outcomes of the Stryker Device in the shoulder, hip, and knee joints 6 months after surgical intervention. * Secondary Objective: To describe clinical outcomes of the Stryker Device in the shoulder, hip, and knee joints 3 months after surgical intervention. * Safety Objective: To describe safety of the Stryker implants in the shoulder, hip, and knee joints 6 months after intervention.
Study Type
OBSERVATIONAL
Enrollment
1,500
Subject has undergone joint space repair using one of the study devices and meets eligibility criteria
Musculoskeletal-Orthopedic Research and Education Foundation
Phoenix, Arizona, United States
RECRUITINGSteadman Hawkins Clinic Denver
Englewood, Colorado, United States
RECRUITINGTSAOG Orthopaedics & Spine
San Antonio, Texas, United States
RECRUITINGASES
Change from baseline
Time frame: 6 months
iHOT-12
Change from baseline
Time frame: 6 months
mHHS
Change from baseline
Time frame: 6 months
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