Investigational Testing of Bodycad Unicompartmental Knee Prosthesis (UKS)
Last updated on July 2021Recruitment
- Recruitment Status
- Recruiting
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Osteoarthritis (Knee)
- Type
- Interventional
- Phase
- Not Applicable
- Design
- Allocation: N/AIntervention Model: Single Group AssignmentIntervention Model Description: Single groupMasking: None (Open Label)Primary Purpose: Treatment
Participation Requirements
- Age
- Between 45 years and 70 years
- Gender
- Both males and females
Description
The patient-specific Bodycad Unicompartmental Knee System will be implanted on patients with knee osteoarthritis of the medial condyle. The study's hypothesis is that personalized shape and fit of patient-specific knee replacement prosthesis will provide a greater stability and a more natural knee m...
The patient-specific Bodycad Unicompartmental Knee System will be implanted on patients with knee osteoarthritis of the medial condyle. The study's hypothesis is that personalized shape and fit of patient-specific knee replacement prosthesis will provide a greater stability and a more natural knee motion in addition to a faster recovery when compared to traditional knee replacement systems. This study is designed to provide a five-years follow-up clinical data on safety and effectiveness of the device.
Tracking Information
- NCT #
- NCT03432481
- Collaborators
- Not Provided
- Investigators
- Principal Investigator: Etienne Belzile, MD CHU de Quebec - Hopital de l'Enfant-Jésus Study Chair: Brian Hamlin, MD Renaissance Orthopedics Study Director: Geoffroy Rivet-Sabourin, PhD Laboratoires Bodycad Inc.
Get Well Soon