Tornier Shoulder Outcomes Study to Examine Safety and Functional Outcomes in Shoulder Arthroplasty and Fracture Patients

Stryker Trauma and Extremities

Status: Active, not recruiting

Conditions: Shoulder Arthroplasty and Fracture Repair

Treatments: Device: Shoulder Arthroplasty

Study type: Observational

Funder types: Industry

Identifiers

NCT02047955

13B-T-SHOULDER-RM

Details and patient eligibility

About

The Tornier Shoulder Outcomes Study is designed to collect safety and efficacy data on designated commercially available Tornier Shoulder repair products. In addition, this study will provide performance data for use in education, marketing materials, peer-reviewed publications and support research and development of future products.

Enrollment: 7,500 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 18 years or older
• Willing and able to comply with the requirements of the study protocol
• Considered for treatment with one or more Tornier shoulder arthroplasty or fracture devices included in this study

Exclusion criteria

• Patients who are not able to comply with the study procedures based on the judgment of the assessor will be excluded (e.g. cannot comprehend study questions, inability to keep scheduled assessment times)