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

Mansoura University20 enrolled

Overview

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

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 Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Class III Malocclusion

Interventions

facemaskDEVICE

Fixation of miniplates by four screws in the maxilla and protraction by using facemask

Eligibility

Sex: ALLMin age: 8 YearsMax age: 13 YearsHealthy volunteers:

Medical Language ↔ Plain English

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.

Locations (1)

Mohamed Adel Raghib

Al Mansurah, Dakahlia Governorate, Egypt

Outcomes

Primary Outcomes

cephalometric radiographs

cephalometric radiographs were analyzed and the amount of maxillary protraction, the dentoskeletal as well the soft tissue changes were evaluated

Time frame: 12 month

Data from ClinicalTrials.gov

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