MedPath

Prefabricated Versus 3D-Printing Myofunctional Appliances

Not Applicable
Conditions
Class II Division 1 Malocclusion
Interventions
Procedure: 3d-Printing Myofunctional Appliance
Registration Number
NCT04810286
Lead Sponsor
T.C. ORDU ÜNİVERSİTESİ
Brief Summary

The aim of this clinical study is to evaluate the dentoskeletal effects of Class II division 1 treatment in growing patients with a prefabricated myofunctional appliance versus a 3D-printing myofunctional appliance.

Detailed Description

This study aims to investigate the dentoskeletal effects of Class II division 1 treatment in growing patients with a prefabricated myofunctional appliance versus a 3D-printing myofunctional appliance.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
120
Inclusion Criteria
  • Increased overjet >4 mm
  • Skeletal Class II relationship (ANB > 4 degree)
  • No previous orthodontic treatment
Exclusion Criteria

-Craniofacial syndrome

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Experimental Group3d-Printing Myofunctional Appliance3D-print myofunctional appliance
Control Group3d-Printing Myofunctional AppliancePrefabricated myfunctional appliance
Primary Outcome Measures
NameTimeMethod
Rate of dentoskeletal changes1 year

Dentoskeletal effects of appliances

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Ordu University

🇹🇷

Ordu, Turkey

© Copyright 2025. All Rights Reserved by MedPath