Clinical Trials Directory

Trials / Completed

CompletedNCT01067651

Comparison of Casting Materials for the Treatment of Clubfoot Using the Ponseti Method

Comparison of Two Different Cast Materials for the Treatment of Congenital Idiopathic Clubfoot Using the Ponseti Method: A Prospective Randomized Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
30 (actual)
Sponsor
Alberta Children's Hospital · Academic / Other
Sex
All
Age
1 Week – 12 Weeks
Healthy volunteers

Summary

The purpose of this study was to determine the influence of cast material on correction of congenital idiopathic clubfeet using the Ponseti method.

Detailed description

Congenital idiopathic clubfoot is the most common congenital deformity in children. It can be a major cause of disability for children, as well as an emotional stress for parents. The Ponseti method of clubfoot correction, consisting of serial manipulations and casting, is now the gold standard of treatment. It has traditionally been described using plaster of Paris (POP) above-knee casts; however, recently semi-rigid fiberglass softcast (SRF, 3M Scotchcast) has grown in popularity. There are currently no randomized controlled trials to prove its efficacy with respect to POP.

Conditions

Interventions

TypeNameDescription
DEVICEPlaster of Paris (POP) casting using the Ponseti Method
DEVICESemi-Rigid Fiberglass softcast using the Ponseti Method

Timeline

First posted
2010-02-11
Last updated
2010-02-11

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01067651. Inclusion in this directory is not an endorsement.