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Agility LP Ankle Arthroplasty Outcomes

NCT01366872 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2012-12-20

Study results available
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Summary

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.

Conditions

  • Rheumatoid Arthritis of Ankle
  • Osteoarthritis of Ankle
  • Traumatic Arthritis of Ankle

Sponsors & Collaborators

  • Orthopaedic Associates of Michigan, PC

    lead OTHER

Principal Investigators

  • John G Anderson, MD · Orthopaedic Associates of Michigan, PC

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-12-31
Primary Completion
2012-08-31
Completion
2012-09-30

Countries

  • United States

Study Locations

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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 NCT01366872 on ClinicalTrials.gov