Three-Dimensional Evaluation of the Airway Space After Distalization in Adults Using Carrière Motion Appliance (CBCT)

February 19, 2022 updated by: Heba Allah Ahmed Ahmed ELghawy, Suez Canal University

Three-Dimensional Evaluation of the Airway Space After Distalization in Adults Using Carrière Motion Appliance: Cone Beam Computed Tomographic Study

Class II malocclusion is quite possibly most continuous treatment issues confronting orthodontists, addressing just about 33% malocclusions. connection between II malocclusion decreased pharyngeal aviation route measurements has been accounted for in writing. few treatment alternatives have been endeavored address this malocclusion, one those choices is distalize maxillary back without extraction treatment. In 2004 another machine presented Luis Carrière conveying his name, called Carrière Motion apparatus. Nonetheless, so far RCT in orthodontic writing assessed impact this machine elements aviation route.

The point this examination assess impact this machine upper aviation route CBCT pictures in treatment post-pubertal patiets dental II malocclusion. near report led comprising 18 members age range from 18-30 years age. treatment impacts assessed radiographically utilizing pre post-distalization CBCT pictures after I connection has been reached. three dimentional investigation performed contemplate impacts distalization upper aviation route. gathered information then genuinely broke down for treatment changes among pre post-distalization.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Patients selected from outpatient center at Department Orthodontics, Faculty Oral Dental Medicine, Suez Canal University. Research Ethical Committee Faculty Oral Dental Medicine, Suez Canal University endorsed this investigation. Patients educated about methodology shown logical, enlivened recordings.

3. Incorporation standards:

The chose patients had met accompanying models:

a) Adults full lasting dentition matured from (18-30). b) Dental II malocclusion beginning from half unit three quarter unit II relationship reciprocally where treatment plan did exclude extraction in upper curve.

c) A ordinary skeletal maxilla typical or gentle direct retrognathic mandible. d) Normal or flat development design. e) All patients ought have great oral cleanliness ought consent inspiration directions give sensible forecast.

f) Absence ejected maxillary third molars. g) The patients should be liberated from any foundational illness or medical conditions.

4. Prohibition models:

  1. Patients set experiences any genuine injury or medical procedure orofacial district.
  2. sex inclination.
  3. No history orthodontic treatment subjects.
  4. No history obstructive breathing issues. 5-Methodology: 5.1 Preoperative intercession:

A Medical History Questionnaire:

A clinical filled patients bar any patients who might be experience ill effects any fundamental illness. Besides, patients checked ear nose throat expert affirm shortfall any aviation route problem.

5.2 Dental Case History Clinical Examination: A total dental case history acquired from every quiet patients analyzed clinically submitted both extraoral intraoral assessment. patients checked meet incorporation measures recently referenced. chose patients who met rules, alluded Periodontal Department centers for additional improvement oral cleanliness Restorative Department Clinics for any necessary fillings lastly alluded Oral Maxillofacial Surgery Department for extraction third maxillary molars in case they completely ejected in oral cavity.

5.3 Patients' Records: The accompanying records acquired from every understanding before endless supply treatment time, 5.3.1 Photographs For every tolerant bunch 4 extraoral 5 intraoral photos taken 5.3.2 Orthodontic Study Models All patients submitted upper lower impressions utilizing alginate impressionA material. wax wafer chomp additionally acquired. Impressions poured promptly utilizing extra hard stone model bases appropriately framed managed orthodontic norms 5.3.3 Cone Beam Computed Tomography: The chose patients submitted two CBCT examines; one pre-usable another after finish distalization utilizing Carrière Motion machine. CBCT pictures procured utilizing SOREDEX SCANORA 3D present in radiology office in Faculty Dentistry Suez Canal University. CBCT examining is performed producer's convention similar administrator. boundaries CBCT set suggestion assembling

Study Type

Interventional

Enrollment (Actual)

18

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Ismailia, Egypt
        • Faculty of Dentistry, Suez Canal University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 30 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

Dental II malocclusion beginning from half unit three quarter unit II relationship reciprocally where treatment plan did exclude extraction in upper curve.

A ordinary skeletal maxilla typical or gentle direct retrognathic mandible. Normal or flat development design. All patients ought have great oral cleanliness ought consent inspiration directions give sensible forecast.

Absence ejected maxillary third molars. The patients should be liberated from any foundational illness or medical conditions.

Exclusion Criteria:

-

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: The motion 3D II appliance
using The motion 3D II appliance on treating Class II orthodontic
The motion 3D II appliance treating class II malocclusion

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Cone Beam Computed Tomography
Time Frame: nine months

CBCT with Nasopharyngeal Airway Nasopharyngeal Airway Volume Oropharyngeal Airway

Oropharyngeal Airway volume Hypopharyngeal Airway Hypopharyngeal Airway volume parameters

nine months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Heba Allah ELghawy, Bachlor, Suez Canal University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 18, 2019

Primary Completion (Actual)

March 15, 2021

Study Completion (Actual)

March 20, 2021

Study Registration Dates

First Submitted

February 19, 2022

First Submitted That Met QC Criteria

February 19, 2022

First Posted (Actual)

March 2, 2022

Study Record Updates

Last Update Posted (Actual)

March 2, 2022

Last Update Submitted That Met QC Criteria

February 19, 2022

Last Verified

February 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 192/2019

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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