The active surveillance post-approval study of the Stelkast Surpass Acetabular System is a retrospective, multi-center, single-arm study intended to collect data on the survivorship and long-term safety and effectiveness of the device.
This active surveillance study is intended to evaluate the survivorship and long-term safety and effectiveness of the Stelkast Surpass Acetabular System. Neither the patient nor the surgeon are blinded to treatment. The study will compare the Surpass' survivorship to the survivorship observed in a historical control group established by a meta-analysis. The evaluation will be conducted for a period of ten years. These evaluations will be recorded through onsite visits and/or mailings sent to physicians requesting deidentified patient-level data for subjects implanted with the Surpass system.
Study Type
OBSERVATIONAL
Enrollment
347
Gill Orthopedic Clinic
Charlotte, North Carolina, United States
Mutschler Orthopedic Institute
Canonsburg, Pennsylvania, United States
Premier Orthopedics and SPM Associates
Glen Mills, Pennsylvania, United States
The Rothman Institute
Philadelphia, Pennsylvania, United States
Survivorship
Time frame: 10 Years
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