The Development of Flat Foot After Ankle Fractures

NCT ID: NCT00507910

Last Updated: 2011-07-21

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

25 participants

Study Classification

OBSERVATIONAL

Study Start Date

2006-12-31

Study Completion Date

2010-12-31

Brief Summary

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In this study we are trying to determine the incidence of flat foot (also called pes planus) among patients who have had an ankle fracture. As compared to the general population, it is predicted that the incidence of pes planus will be higher among people who have fractured their ankle.

Detailed Description

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Pes planus may develop following ankle fractures due to additional injuries that are sustained at the time of ankle fracture. If this study can demonstrate an association, further research would investigate how to effectively treat the pes planus early to prevent it from becoming a symptomatic problem.

Conditions

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Pes Planus

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

Patients will be considered eligible if:

* They have sustained Weber type B or C ankle fractures and needed open reduction
* They are 18 years of age or older
* They are expected to be full weight bearing for at least 4 months to allow the potential of supporting structures to stretch and pes planus to develop

Exclusion Criteria

* Patients will be excluded if they already have flat foot in their non-fractured foot.
* Patients with bilateral ankle fractures
* Patients who are not competent to sign a consent form
* A second fracture to the ankle
* Pathological fractures
* Patients with underlying cancer.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ottawa Hospital Research Institute

OTHER

Sponsor Role lead

Responsible Party

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Ottawa Hospital Research Institute

Principal Investigators

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Alan Giachino

Role: PRINCIPAL_INVESTIGATOR

OHRI

Locations

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The Ottawa Hospital

Ottawa, Ontario, Canada

Site Status

Countries

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Canada

Other Identifiers

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OHREB2006542

Identifier Type: -

Identifier Source: org_study_id

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