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

NCT02002637 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 11

Last updated 2017-04-28

No results posted yet for this study

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.

Conditions

Interventions

DEVICE

Latella Knee Implant System

Sponsors & Collaborators

  • Cotera, Inc.

    lead INDUSTRY

Principal Investigators

  • Manoj Ramachandran, MD · Barts & The London NHS Trust

Study Design

Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
30 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-11-30
Primary Completion
2015-09-30
Completion
2017-04-30

Countries

  • Netherlands
  • United Kingdom

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02002637 on ClinicalTrials.gov