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

NCT01067651 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2010-02-11

No results posted yet for this study

Summary

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

Conditions

  • Clubfoot
  • Ponseti Method
  • Talipes Equinovarus
  • Casting

Interventions

DEVICE

Plaster of Paris (POP) casting using the Ponseti Method

DEVICE

Semi-Rigid Fiberglass softcast using the Ponseti Method

Sponsors & Collaborators

  • Alberta Children's Hospital

    lead OTHER

Principal Investigators

  • Jason Howard, MD · IWK Health Centre

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
1 Week
Max Age
12 Weeks
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Countries

  • Canada

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01067651 on ClinicalTrials.gov