SportsPro: Post-Market Clinical Follow Up Study

Stryker

Status: Enrolling

Conditions: Hip Injuries; Knee Injuries; Shoulder Injuries

Treatments: Device: Standard of Care Treatment

Study type: Observational

Funder types: Industry

Identifiers

NCT06320925

SYK-SM-2022-02

Details and patient eligibility

About

Retrospective, multi-center, chart review (only to include data that is part of the surgeons' standard practice)

Full 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.

Enrollment: 1,500 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

1,500 participants in 1 patient group

Study Subjects

Description:

Patients who have undergone a surgical procedure (per product indications for use) using the Stryker implants who meet all of the following criteria will be screened and enrolled by participating Investigators.

Treatment:

Device: Standard of Care Treatment