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

N/ATerminatedNCT02002637

Cotera, Inc.11 enrolled

Overview

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.

Study Type

INTERVENTIONAL

Allocation

Purpose

DEVICE_FEASIBILITY

Masking

NONE

Enrollment

Conditions

Osteoarthritis

Interventions

Latella Knee Implant SystemDEVICE

Eligibility

Sex: ALLMin age: 30 YearsMax age: 65 Years

Medical Language ↔ Plain English

Inclusion Criteria: * History of pain as due to medial osteoarthritis Exclusion Criteria: * Rheumatoid arthritis * Joint or ligament instability * Metal ion allergy

Locations (2)

Slotervaart Hospital

Amsterdam, Netherlands

Barts Health NHS Trust

London, United Kingdom

Outcomes

Primary Outcomes

Freedom from unanticipated serious adverse device effects

Time frame: 12 Months

Data from ClinicalTrials.gov

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