Treating Gnathic Form of Mesial Occlusion in Early Adolescence Patients

Treating Gnathic Form of Mesial Occlusion in Early Adolescence Patients: A Clinical Trial

The primary purpose of this study was to evaluate the immediate and previous results of the effectiveness of non-surgical orthopedic treatment in children aged 12-14 years with gnathic forms of mesial occlusion by the method of dentoalveolar compensation using a permanent apparatus with a palatal expanding screw.

Study Overview

• Status: Completed
• Conditions: Gnathic (Skeletal) Mesial Occlusion
• Intervention / Treatment: Device: dentoalveolar compensation method; Device: face mask

• Study Type: Observational
• Enrollment (Actual): 46

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 12 years to 14 years (Child)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

• Sampling Method: Probability Sample

Study Population

To evaluate the early and late results of the non-surgical orthopedic treatment efficiency in 12-14 years old children with the gnathic forms of mesial occlusion by the dentoalveolar compensation utilizing a permanent device with a palatal expanding screw.

Description

Inclusion Criteria:

patients with a gnathic (skeletal) mesial occlusion patients age 12-14 years patients who underwent orthopedic treatment

Exclusion Criteria:

change of residence severe form of gnathic mesial occlusion congenital anomalies of the dento-maxillo-facial area

Study Plan

How is the study designed?

Number of groups / cohorts

2

Cohorts and Interventions

Group / Cohort	Intervention / Treatment
The experimental group; The experimental group included 26 patients - orthopedic treatment was performed using the dentoalveolar compensation method with permanent apparatus with a palatal expanding screw.	Device: dentoalveolar compensation method; orthopedic treatment was performed using the dentoalveolar compensation method with permanent apparatus with a palatal expanding screw
The comparison group; The comparison group included 20 patients - orthopedic treatment was performed using a face mask.	Device: face mask; orthopedic treatment was performed using a face mask.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
dentoalveolar compensation method	orthopedic treatment was performed using the dentoalveolar compensation method with permanent apparatus with a palatal expanding screw	2014-2020
face mask	orthopedic treatment was performed using a face mask	2014-2020

Collaborators and Investigators

• Sponsor: The 108 Military Central Hospital

Study record dates

Study Major Dates

• Study Start (Actual): September 5, 2014
• Primary Completion (Actual): October 5, 2020
• Study Completion (Actual): October 5, 2020

Study Registration Dates

• First Submitted: December 14, 2021
• First Submitted That Met QC Criteria: December 23, 2021
• First Posted (Actual): December 29, 2021

Study Record Updates

• Last Update Posted (Actual): December 29, 2021
• Last Update Submitted That Met QC Criteria: December 23, 2021
• Last Verified: December 1, 2021

More Information

Terms related to this study

• Keywords: orthodontic treatment; early adolescence; orthodontic practice
• Other Study ID Numbers: Le Thi Thu Hai

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO
• IPD Plan Description: The study was anonymous. No personal data will be revealed

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No