RECRUITING

Exactech Vantage Total Ankle System Post Market Clinical Follow-Up - US Only

Description

The objectives of this study are to evaluate the performance and safety of the Vantage Total Ankle System. This study will follow subjects for a period of up to 10 years post-surgery.

Study Overview

Study Details

Study overview

The objectives of this study are to evaluate the performance and safety of the Vantage Total Ankle System. This study will follow subjects for a period of up to 10 years post-surgery.

An Open Label, Multi-Center, Single Arm Prospective Evaluation of Exactech Vantage Total Ankle System

Exactech Vantage Total Ankle System Post Market Clinical Follow-Up - US Only

Condition
Ankle Rheumatoid Arthritis
Intervention / Treatment

-

Contacts and Locations

Durham

Duke University Medical Center, Durham, North Carolina, United States, 27703

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Patient is indicated for total ankle arthroplasty
  • * Patient is skeletally mature
  • * Patient is mentally capable of completing follow-up forms
  • * Patient will be available for follow-up out to 10 years
  • * Patient has been deemed a candidate for Ankle replacement by diagnosis of the investigator
  • * Patient is willing and able to read and sign a study informed consent form
  • * Patient with excessive bone loss at the ankle joint site
  • * Patient with severe osteoporosis
  • * Patient with complete talar avascular necrosis
  • * Patient with Active Osteomyelitis
  • * Patient with Infection at the ankle site or infection at distant sites that could migrate to the ankle
  • * Patient with Sepsis
  • * Patient with Vascular deficiency in the involved limb
  • * Patient with Neuromuscular inadequacy (e.g. Prior paralysis, fusion and or inadequate abductor strength)
  • * Patient with Neuropathic joints
  • * Patient with Neurological or musculoskeletal disease or loss of function that may adversely affect movement of the lower limb, gait, or weight bearing
  • * Patient with Poor soft tissue coverage around the ankle
  • * Patient with Charcot arthropathy
  • * Previous ankle arthrodesis with excision of the malleoli
  • * Excessive loads as caused by activity or patient weight - per investigator discretion
  • * Skeletally immature patients (patient is less than 21 years if age at time of surgery)
  • * Patient with dementia
  • * Patient with known metal allergies
  • * Patient who is pregnant

Ages Eligible for Study

21 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Exactech,

Study Record Dates

2031-09-30