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 — DEVICE
    a 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

Locations (1)

FacilityCityStateZIPSite coordinators
UW-Health Pediatric Orthopedics ClinicsMadisonWisconsin53792-

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