Feasibility of the Latella Implant System for Medial Osteoarthritis (OA)
This trial is active, not recruiting.
|Treatment||latella knee implant system|
|Start date||November 2013|
|End date||September 2015|
|Trial identifier||NCT02002637, COT1-13-01, COTERA-1|
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.
|United States||No locations recruiting|
|Other Countries||No locations recruiting|
Freedom from unanticipated serious adverse device effects
time frame: 12 Months
Male or female participants from 30 years up to 65 years old.
Inclusion Criteria: - History of pain as due to medial osteoarthritis Exclusion Criteria: - Rheumatoid arthritis - Joint or ligament instability - Metal ion allergy
|Official title||Evaluation of the Latella Implant System for Lateralization of the Iliotibial Band to Offload the Medial Condyle for Pain Relief in Patients With Medial Osteoarthritis - A Safety Study|
|Principal investigator||Manoj Ramachandran, MD|
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