Actively Recruiting
3D Evaluation of Maxillary Expansion Methods
Led by Büşra Zeynep Yörük · Updated on 2025-12-04
60
Participants Needed
1
Research Sites
27 weeks
Total Duration
On this page
Sponsors
B
Büşra Zeynep Yörük
Lead Sponsor
C
Centerdent Orthodontics & Aesthetic Dentistry Clinic
Collaborating Sponsor
AI-Summary
What this Trial Is About
This controlled prospective clinical trial aims to evaluate the effectiveness of different maxillary expansion methods in children with maxillary transverse deficiency. A total of 60 participants will be included: 20 patients will receive Invisalign Palatal Expander (IPE), 20 will receive acrylic cap splint Rapid Maxillary Expansion (RME), and 20 will serve as an untreated control group. Three-dimensional (3D) intraoral and extraoral scans will be taken at the end of expansion, at 3 months, and at 6 months. Primary outcomes include maxillary arch width, first molar angulation, palatal surface area, and palatal volume. Secondary outcomes include soft tissue changes in the facial region. This study provides a direct comparison between a traditional and a modern digital expansion method, generating evidence for clinical decision-making in pediatric orthodontics.
CONDITIONS
Official Title
3D Evaluation of Maxillary Expansion Methods
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Children aged 6-12 years
- Good oral hygiene and adequate patient cooperation
- No previous orthodontic expansion treatment
You will not qualify if you...
- Systemic diseases affecting growth, bone metabolism, or craniofacial development
- Craniofacial syndromes or congenital anomalies
- Severe behavioral or cooperation problems
- Previous orthodontic or orthopedic maxillary expansion
- Patients undergoing medications that affect bone metabolism
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Bezmialem Vakif University
Istanbul, Fatih, Turkey (Türkiye), 34093
Actively Recruiting
Research Team
B
Banu Kılıç, Associate Professor
CONTACT
B
Büşra Zeynep Yörük, Phd Student
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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