Comparing Outcomes and Complications Following Mastisol Application for Clubfoot Casting
Part of paid clinical trials in Madison, Wisconsin.
- Sponsor
- University of Wisconsin, Madison
- Study ID
- NCT07154550
- Status
- Recruiting
Conditions
- Club Foot
Eligibility Criteria
- Sex
- ALL
- Age
- 0 Weeks - 12 Weeks
- Healthy Volunteers
- Not accepted
Interventions
- Mastisol — DEVICEa liquid adhesive used to secure dressings for extended periods of time
Study Details
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.
Key Dates
- Start date
- Feb 11, 2026
- Status verified
- Feb 2026
- Primary completion
- Nov 30, 2032
- Completion
- Nov 30, 2032
Study Design
- Enrollment
- 100 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Leg with Mastisol
- No Intervention: Control Leg
Primary Outcome Measure
Number of Weeks Need to Obtain Correction [ Time Frame: up to 12 weeks ]
Central Contacts
- Ava Barker(608)-263-2356
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| UW-Health Pediatric Orthopedics Clinics | Madison | Wisconsin | 53792 | - |
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