Prefabricated Versus 3D-Printing Myofunctional Appliances

T.C. ORDU ÜNİVERSİTESİ

Status: Unknown

Conditions: Class II Division 1 Malocclusion

Treatments: Procedure: 3d-Printing Myofunctional Appliance

Study type: Interventional

Funder types: Other

Identifiers

NCT04810286

2021-47

Details and patient eligibility

About

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.

Full 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.

Enrollment: 120 estimated patients

Sex: All

Ages: 8 to 12 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Increased overjet >4 mm
• Skeletal Class II relationship (ANB > 4 degree)
• No previous orthodontic treatment

Exclusion criteria

-Craniofacial syndrome

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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120 participants in 2 patient groups

Experimental Group

Experimental group

Description:

3D-print myofunctional appliance

Treatment:

Procedure: 3d-Printing Myofunctional Appliance

Control Group

Active Comparator group

Description:

Prefabricated myfunctional appliance

Treatment:

Procedure: 3d-Printing Myofunctional Appliance