Palatal Versus Buccal Protraction Using Plates Assisted With Facemask in Growing Class III Patients

Not Applicable

Completed

• Conditions: Class III Malocclusion
• Interventions: Device: facemask

• Registration Number: NCT06452368
• Lead Sponsor: Mansoura University

Brief Summary

to compare Palatal and buccal protraction using plates assisted with facemask in growing class III patients

Detailed Description

A randomized controlled clinical trial was adopted in this study. A total of 20 growing Class III patients were selected from patients seeking orthodontic treatment. The participants were recruited from the department of Orthodontics at Faculty of Dentistry, Mansoura University. No active advertisement was used for participant recruitment, and instead, a convenience sample was formed. Prior to participating in the study, the purpose of the study was explained to the parents of the children and informed consents and assents were obtained according to the guidelines on human research adopted by the Research Ethics Committee Faculty of Dentistry, Mansoura University

Study Timeline

• Study Start: 2022-10-01
• Primary Completion: 2023-11-01
• Study Completion: 2023-11-20
• Status Verified: 2024-06
• Study First Submitted: 2024-06-05
• Study First Submitted QC: 2024-06-05
• Study First Posted: 2024-06-11
• Last Update Submitted: 2024-06-12
• Last Update Posted: 2024-06-14

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

• Growing patients with age ranged between 8-13 years old.
• Patients should have examination: Class III malocclusion due to maxillary retrusion as verified by clinical and radiographic examination; SNA <79 and ANB angle < -1.
• Good likelihood of recall availability.

Exclusion Criteria

• Vertical skeletal mal relationship.
• History of previous orthodontic/orthopedic treatment.
• Bad habits that may jeopardize the appliance.
• Patients with systemic diseases
• Congenital deformities such as cleft lip and/or palate.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Buccal protraction	facemask	Buccal plate assisted with facemask
Palatal protraction	facemask	Palatal plate assisted with facemask

Primary Outcome Measures

Name	Time	Method
cephalometric radiographs	12 month	cephalometric radiographs were analyzed and the amount of maxillary protraction, the dentoskeletal as well the soft tissue changes were evaluated

Trial Locations

Locations (1)

Mohamed Adel Raghib; 🇪🇬 Mansoura, Dakahlia, Egypt