Evaluation of the Latella™ Knee Implant System for Medial Osteoarthritis Pain Reduction (Latella-US)

C

Cotera

Status

Terminated

Conditions

Osteoarthritis

Treatments

Device: Latella Knee Implant System

Study type

Interventional

Funder types

Industry

Identifiers

NCT02608957
CIP-0002

Details and patient eligibility

About

The objective of the Latella-US study is to demonstrate the safety and efficacy of the Latella Knee Implant System for the reduction of medial osteoarthritis pain.

Enrollment

1 patient

Sex

All

Ages

30 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • History of pain due to medial osteoarthritis
  • Qualifying baseline pain scores
  • Kellgren-Lawrence Grades 2-3

Exclusion criteria

  • Osteoporosis
  • Rheumatoid arthritis
  • Joint instability
  • Metal ion allergy
  • Permanent implant in or around the knee joint
  • Prior anterior cruciate ligament reconstruction

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

1 participants in 1 patient group

Latella Knee Implant System
Experimental group
Treatment:
Device: Latella Knee Implant System

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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