Feasibility of the Latella Implant System for Medial Osteoarthritis (OA)

Cotera

Status: Terminated

Conditions: Osteoarthritis

Treatments: Device: Latella Knee Implant System

Study type: Interventional

Funder types: Industry

Identifiers

NCT02002637

COT1-13-01

COTERA-1

Details and patient eligibility

About

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.

Enrollment: 11 patients

Sex: All

Ages: 30 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• History of pain as due to medial osteoarthritis

Exclusion criteria

• Rheumatoid arthritis
• Joint or ligament instability
• Metal ion allergy

Trial design

Primary purpose: Device Feasibility

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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11 participants in 1 patient group

Latella Knee Implant System

Experimental group

Treatment:

Device: Latella Knee Implant System