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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03580746
Other study ID # UZLeuvenColette
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date September 2014
Est. completion date August 2015

Study information

Verified date March 2021
Source Universitaire Ziekenhuizen Leuven
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

There are many different treatments of congenital talipes equinovarus. At our institution, the investigators use the Ponseti method with manipulation and immobilization of the foot. In this study the investigators should like to demonstrate the better outcome in clinical results and in gait analysis of patients treated with the Ponseti method, compared to the 'older' methods of taping and posteromedial release.


Description:

There are many different treatments of congenital talipes equinovarus. At our institution, the investigators use the Ponseti method with manipulation and immobilization of the foot. In this study the invistigators should like to demonstrate the better outcome in clinical results and in gait analysis of patients treated with the Ponseti method, compared to the 'older' methods of taping and posteromedial release. Trial objectives With this study the investigators would like to investigate whether clinical results and gait analysis in patients treated with Ponseti has better results compared to patients treated with the older methods.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date August 2015
Est. primary completion date June 2015
Accepts healthy volunteers No
Gender All
Age group N/A to 18 Years
Eligibility Inclusion Criteria: - All patients with talipes equinovarus who have been treated at our institution Exclusion Criteria: - Patients with other disorders which may influence the clinical or gait analysis outcome

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Taping and posteromedial release

Ponseti


Locations

Country Name City State
Belgium University Hospitals of Leuven Pellenberg Vlaams-Brabant

Sponsors (1)

Lead Sponsor Collaborator
Universitaire Ziekenhuizen Leuven

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical results Different clinical results between the two groups using AOFAS (American Orthopaedic Foot and Ankle Society) score. 1 year
Secondary Gait analysis Differences in gait analysis between the two groups. While walking barefoot following parameters will be compared: ranges of motion occurring at each joint and each sub phase of stance 1 year
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