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
Group Intervention Description Experimental Group 3d-Printing Myofunctional Appliance 3D-print myofunctional appliance Control Group 3d-Printing Myofunctional Appliance Prefabricated myfunctional appliance
- Primary Outcome Measures
Name Time Method Rate of dentoskeletal changes 1 year Dentoskeletal effects of appliances
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Ordu University
🇹🇷Ordu, Turkey