Feasibility of the Latella Implant System for Medial Osteoarthritis (OA)
Not Applicable
Terminated
- Conditions
- Osteoarthritis
- Interventions
- Device: Latella Knee Implant System
- Registration Number
- NCT02002637
- Lead Sponsor
- Cotera, Inc.
- Brief Summary
The objective of this study is to evaluate the safety and technical feasibility of implanting the Latella Implant System in the treatment of patients with medial osteoarthritis of the knee.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 11
Inclusion Criteria
- History of pain as due to medial osteoarthritis
Exclusion Criteria
- Rheumatoid arthritis
- Joint or ligament instability
- Metal ion allergy
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Latella Knee Implant System Latella Knee Implant System -
- Primary Outcome Measures
Name Time Method Freedom from unanticipated serious adverse device effects 12 Months
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (2)
Slotervaart Hospital
🇳🇱Amsterdam, Netherlands
Barts Health NHS Trust
🇬🇧London, United Kingdom