A Retrospective Study to Assess the Outcome After Surgical Reconstruction of the Midfoot With the Midfoot Fusion Bolt in Patients With Neuroarthropathy

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

47 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-01-31

Study Completion Date

2014-05-31

Brief Summary

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The aim of this study is to investigate the clinical outcomes of surgical correction of foot deformity with the MFB in a larger group of patients with neurological impairment of the foot.

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Detailed Description

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Conditions

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Charcot Neuroarthropathy Diabetic Foot

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Study Groups

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MFB

Surgical arthrodesis of the midfoot with the Midfoot Fusion Bolt (MFB)

MFB

Intervention Type PROCEDURE

Surgical arthrodesis of the midfoot with the Midfoot Fusion Bolt (MFB)

Interventions

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MFB

Surgical arthrodesis of the midfoot with the Midfoot Fusion Bolt (MFB)

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Age ≥ 18 at date of inclusion
* Previous surgical reconstruction of the midfoot with Midfoot Fusion Bolt(s) for one of the following indications:

Neuroarthropathy Deformity of the foot with neurological impairment - Signed informed consent according to local regulation