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Agility LP Ankle Arthroplasty Outcomes

O

Orthopaedic Associates of Michigan, PC

Status

Completed

Conditions

Rheumatoid Arthritis of Ankle
Osteoarthritis of Ankle
Traumatic Arthritis of Ankle

Study type

Observational

Funder types

Other

Identifiers

NCT01366872
OAM-LP-2010

Details and patient eligibility

About

This is a research study which is being done to determine the outcomes following Agility LP ankle replacement. This implant was approved by the FDA in 2007 and has been used since then with good early results. You are being asked to volunteer for this study because you have undergone Total Ankle Arthroplasty with Agility LP prosthesis. The purpose of the study is to compare the range of motion, level of pain and function during daily living prior to and after your ankle surgery.

Enrollment

50 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Over 18 years old
  • Can comprehend and sign the informed consent
  • Patient must have undergone Agility LP ankle replacement between January 2006 to June 2008

Exclusion criteria

  • Patient has had following procedures on the study limb within two years of TAA
  • Revision of TAA
  • Ankle arthrodesis
  • Amputation
  • Agility LP arthroplasty was done as a revision procedure for a failed TAA or as a takedown of ankle fusion.
  • Any condition that, in the opinion of the investigator, makes the patient unsuitable for participation in the study.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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