Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00152334
Other study ID # C01-0210
Secondary ID W01-0057
Status Completed
Phase N/A
First received
Last updated
Start date September 2005
Est. completion date October 2018

Study information

Verified date May 2017
Source University of British Columbia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study was to determine the efficacy of adding Botox injection to serial manipulations and castings in patients with clubfoot. The study hypothesis was that the use of Botox in the setting of serial manipulations and castings is an effective treatment for clubfoot.


Description:

All patients meeting the inclusion criteria will undergo manipulation and casting until hindfoot stall is encountered. Hindfoot stall is defined as forefoot abduction to 60 degrees but persistence of hindfoot equinus. At hindfoot stall, subjects received Botox injections at 10 IU/kg into the gastrosoleus muscle complex. Following injections, subjects were recasted.


Recruitment information / eligibility

Status Completed
Enrollment 500
Est. completion date October 2018
Est. primary completion date March 2016
Accepts healthy volunteers No
Gender All
Age group N/A to 2 Years
Eligibility Inclusion Criteria: 1. Children presenting with idiopathic clubfoot/feet at BC Children's Hospital 2. Children ranging in age from 1 day to 2 years old at initial treatment Children who have had previous intervention for their clubfoot (methods including surgery, Ponseti method, Kite method, physical therapy method) and had a clubfoot recurrence requiring re-intervention

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Botox
All patients meeting the inclusion criteria will undergo manipulation and casting until hindfoot stall is encountered. Hindfoot stall is defined as forefoot abduction to 60 degrees but persistence of hindfoot equinus. At hindfoot stall, subjects received Botox injections at 10 IU/kg into the gastrosoleus muscle complex. Following injections, subjects were recasted.

Locations

Country Name City State
Canada BC Children's Hospital, Department of Orthopaedics Vancouver British Columbia

Sponsors (1)

Lead Sponsor Collaborator
University of British Columbia

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary The rate of successful clubfoot correction from a single Botox injection. This coincides with entrance into Boots and Bars. This was measured 8 weeks following injection. 8 weeks
Secondary Secondary outcomes of the study as outlined in protocol (include time of measurement) See protocol
Secondary Secondary Outcomes: Patient outcomes collected at every patient visit including: See protocol
Secondary 1. Ankle range of motion (dorsiflexion and plantarflexion) (collected at every visit) See protocol
Secondary 2. Heel Bisector Scores (collected at every visit) See protocol
Secondary 3. Pedobarographs (every 6 months from 18 months to 5 years) See protocol
Secondary Gait Analysis (every 2 years from 5 years of age until skeletal maturity) See protocol
See also
  Status Clinical Trial Phase
Completed NCT00152347 - A Double-Blind, Randomized Control Trial Comparing Botulinum Toxin Type A (Botox) and Placebo in the Treatment of Idiopathic Clubfoot N/A