Wright Foot & Ankle Post-Market Observational Study

Stryker Trauma and Extremities

Status: Terminated

Conditions: Fusion of Joint; Fracture; Arthritis; Trauma Injury; Rheumatoid Arthritis

Treatments: Device: Foot and Ankle Devices

Study type: Observational

Funder types: Industry

Identifiers

NCT04118894

INT19-MDR-001

Details and patient eligibility

About

WRIGHT FOOT & ANKLE POST-MARKET OBSERVATIONAL STUDY, Multi-Year, Multi-Site, Multi-Device, Post-Market Observational Study, 10 sites, a minimum of 40 patients per device

Full description

The selected design is a global, multi-center, non-randomized, prospective observational study. The study subjects included are those treated with one or more approved or cleared Wright Medical products included in this study.

Enrollment: 119 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Willing and able to consent to participate (written, informed consent);
• Willing and able to attend/complete the requested follow-up visits;
• Considered for treatment with one or more approved or cleared Wright Medical products included in this study

Exclusion criteria

• Subjects determined, by the investigator, to be an inappropriate candidate for the procedure indicated;
• Unable to consent to participate (written, informed consent);
• Unable to attend/complete the requested follow-up visits

Trial design

119 participants in 1 patient group

Foot and Ankle Devices

Description:

The study subjects included are those treated with one or more approved or cleared Wright Medical products included in this study.

Treatment:

Device: Foot and Ankle Devices