NCT06320925

SportsPro: Post-Market Clinical Follow Up Study

A Retrospective, Multi-Center, Post-Market Clinical Follow-Up Study of Stryker Class IIb Implants

• Status: Recruiting
• Phase: —
• Study type: Observational
• Enrollment: 1,500 (estimated)
• Sponsor: Stryker Endoscopy · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

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.

Conditions

• Shoulder Injuries
• Knee Injuries
• Hip Injuries

Interventions

Type	Name	Description
DEVICE	Standard of Care Treatment	Subject has undergone joint space repair using one of the study devices and meets eligibility criteria

Timeline

• Start date: 2023-12-05
• Primary completion: 2026-06-30
• Completion: 2026-12-01
• First posted: 2024-03-20
• Last updated: 2025-05-29

Locations

3 sites across 1 country: United States

Regulatory

• FDA-regulated device study