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

A

AO Clinical Investigation and Publishing Documentation

Status

Completed

Conditions

Diabetic Foot
Charcot Neuroarthropathy

Treatments

Procedure: MFB

Study type

Observational

Funder types

Other

Identifiers

NCT01770639
MFB Retro

Details and patient eligibility

About

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.

Enrollment

47 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Exclusion criteria

  • Prisoner at date of inclusion

Trial design

47 participants in 1 patient group

MFB
Description:
Surgical arthrodesis of the midfoot with the Midfoot Fusion Bolt (MFB)
Treatment:
Procedure: MFB

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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