Hip Injuries, Knee Injuries, Shoulder Injuries
Conditions
Brief summary
Retrospective, multi-center, chart review (only to include data that is part of the surgeons' standard practice)
Detailed description
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.
Interventions
DEVICEStandard of Care Treatment
Subject has undergone joint space repair using one of the study devices and meets eligibility criteria
Sponsors
Stryker Endoscopy
Study design
Observational model
OTHER
Time perspective
RETROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Subject was ≥ 18 years of age at the time of the surgery 2. Subject has undergone joint space repair using one of the study devices
Exclusion criteria
1. Subjects who are less than 6 months post-intervention 2. Concurrent participation in an investigational clinical study during the study period
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| ASES | 6 months | Change from baseline |
| iHOT-12 | 6 months | Change from baseline |
| mHHS | 6 months | Change from baseline |
Countries
United States
Contacts
Primary ContactHayley Taylor, MS
Backup ContactColleen Roden, MS
Outcome results
None listed