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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00507910
Other study ID # OHREB2006542
Secondary ID
Status Completed
Phase N/A
First received July 25, 2007
Last updated July 19, 2011
Start date December 2006
Est. completion date December 2010

Study information

Verified date July 2011
Source Ottawa Hospital Research Institute
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Observational

Clinical Trial Summary

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.


Description:

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.


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date December 2010
Est. primary completion date December 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Canada The Ottawa Hospital Ottawa Ontario

Sponsors (1)

Lead Sponsor Collaborator
Ottawa Hospital Research Institute

Country where clinical trial is conducted

Canada, 

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