Trials / Active Not Recruiting
Active Not RecruitingNCT03720782
Safety and Performance Study of the Legion Porous System in Total Knee Arthroplasty
Multi-center Study of the Safety and Performance of Primary Total Knee Arthroplasty With LEGION™ Porous HA Tibial Baseplates (With and Without Holes) and/or the LEGION™ Porous HA CR Femoral Component in US Centers
- Status
- Active Not Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 118 (actual)
- Sponsor
- Smith & Nephew, Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this research is to collect data on patients that had the Legion Porous HA Tibial Baseplates and/or the Legion Porous HA Femoral component implanted in the past. Smith \& Nephew will evaluate the safety and performance of these implants for 10 years post-surgery.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | LEGION Porous HA Tibial Baseplate and/or the LEGION Porous HA CR Femoral Component | LEGION Porous HA Tibial Baseplate (with and without holes) and/or the LEGION Porous HA CR Femoral Component |
Timeline
- Start date
- 2019-05-22
- Primary completion
- 2031-01-23
- Completion
- 2032-12-31
- First posted
- 2018-10-25
- Last updated
- 2024-04-02
Locations
2 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03720782. Inclusion in this directory is not an endorsement.