Anterior Tibiotalar Arthrodesis With Blade Plate Fixation

Withdrawn

• Conditions: Arthritis; Pilon Fracture

• Registration Number: NCT01818466
• Lead Sponsor: University of Utah

Brief Summary

The aim of this study is to evaluate the clinical and radiographic outcomes of patients who have previously undergone tibiotalar arthrodesis using an anterior approach with blade-plate fixation for tibiotalar arthritis secondary to injury to the articular surface of the distal tibia.

Detailed Description

Not available

Basic Information
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Recruitment & Eligibility
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Study & Design

Study Timeline

• Study Start: 2012-11
• Study First Submitted: 2013-02-05
• Study First Submitted QC: 2013-03-21
• Study First Posted: 2013-03-26
• Primary Completion: 2016-05
• Study Completion: 2016-05
• Status Verified: 2016-06
• Last Update Submitted: 2016-06-27
• Last Update Posted: 2016-06-28

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• All patients whom have undergone anterior ankle arthrodesis with a blade plate construct, performed by a single surgeon, between January 2003 and July 2011 at the University of Utah or Primary Childrens Medical Center (PCMC) will be eligible for inclusion.

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Exclusion Criteria

• Any patient who is not 18 years of age or older will not be eligible for the study.

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Outcome Questionnaires relating to the patients current condition	1 Year after Surgery	These questionnaires will include the FAOS, FADI, SF-36, PromisCAT, SMFA, and the DRAM.