Actively Recruiting
Comparing Outcomes and Complications Following Mastisol Application for Clubfoot Casting
Led by University of Wisconsin, Madison · Updated on 2026-02-19
100
Participants Needed
1
Research Sites
350 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study is to assess if the application of Mastisol, a liquid adhesive, improves outcomes during bilateral clubfoot casting and reduces complications and development of complex clubfoot for the duration of their casting and up to 5 years follow-up.
CONDITIONS
Official Title
Comparing Outcomes and Complications Following Mastisol Application for Clubfoot Casting
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with bilateral clubfeet
- Starting standard of care treatment with the Ponseti method between 0-12 weeks of age
- For patients born prematurely, eligibility age will be based on corrected gestational age
- At least one parent or guardian able to converse, read, and write in English
You will not qualify if you...
- Patients without bilateral clubfoot
- Patients starting treatment for clubfoot after 12 weeks of age
- Parents or guardians unable to converse, read, and write in English
- Parents or guardians who do not or cannot provide informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
UW-Health Pediatric Orthopedics Clinics
Madison, Wisconsin, United States, 53792
Actively Recruiting
Research Team
A
Ava Barker
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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