Actively Recruiting
Efficacy of 3D-Printed Mouth Splints
Led by Wake Forest University Health Sciences · Updated on 2025-12-17
10
Participants Needed
1
Research Sites
92 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The study will investigate the effectiveness of a 3D-printed mouth splint designed to increase dimensions of oral aperture and reduce disability associated with mouth contractures. The validated Mouth Impairment and Disability Assessment (MIDA) survey will be used to objectively measure patient progress in functionality and quality of life.
CONDITIONS
Official Title
Efficacy of 3D-Printed Mouth Splints
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients 2 years to 99 years of age with documented microstomia following burn injuries.
- Ability to comply with prescribed home exercises and follow-up visits.
You will not qualify if you...
- Cognitive or physical inability to perform the prescribed exercises.
- Inability of a caretaker to be able to deliver therapy daily.
- Concomitant conditions that may significantly affect oral aperture (e.g., temporomandibular joint (TMJ) disorders).
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Wake Forest University Health Sciences
Winston-Salem, North Carolina, United States, 27157
Actively Recruiting
Research Team
S
Study Coordinator
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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