The Effect of Different Treatment Modalities of Class II Malocclusion on Upper Third Molars.

October 22, 2023 updated by: Amira Aboalnaga, Cairo University

The Effect of Different Treatment Modalities of Class II Malocclusion on Upper Third Molars: A Retrospective Longitudinal Study

What is the effect of the different treatment modalities (distalization versus upper premolar extraction) of class II malocclusion on the position, inclination and incidence of impaction of the upper third molars?

Study Overview

Status

Completed

Detailed Description

What is the effect of the different treatment modalities (distalization versus upper premolar extraction) of class II malocclusion on the position, inclination and incidence of impaction of the upper third molars? Pico P: Adolescent patients with class II malocclusion having bilateral developing upper third molars.

I: bilateral upper first premolar extraction orthodontic treatment with moderate anchorage.

C: distalization orthodontic treatment. O: Primary: angulation of the maxillary third molars.

Study Type

Observational

Enrollment (Actual)

46

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

      • Cairo, Egypt, 12588
        • Amira Aboalnaga

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

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

• Egyptian Adolescent males and females (16 -18 years)

Description

Inclusion Criteria:

  • Adolescent males and females (16 -18 years) with Bilaterally developing maxillary third molars. Not more than two thirds of the root development of the third molars had taken place.
  • Class II malocclusion cases that were treated by 1) maxillary premolar extraction with a moderate anchorage requirement and achieved full unit class II molar relationship or 2) Distalization treatment plan and class I molar relationship was achieved.
  • Patients with high-quality pre- and post-treatment radiographs.
  • Normal or increased vertical dimension.

Exclusion Criteria:

  • Maxillary Premolar extraction cases requiring maximum anchorage preparation.
  • Low vertical dimension.
  • Patients without dentofacial deformities, severe facial asymmetries, microdontia or hypodontia.

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
extraction treatment
patients treated with bilateral upper first premolar extraction orthodontic treatment with moderate anchorage.
bilateral upper first premolar extraction orthodontic treatment with moderate anchorage.
distalization treatment
patients treated by distalization orthodontic treatment.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The angulation of the maxillary third molars.
Time Frame: up to 24 weeks.
the angle between the long axis of the third molar and the palatal plane
up to 24 weeks.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The vertical position of the third molars
Time Frame: up to 24 weeks
the vertical position of the third molar relative to the second molar measured using Archer classification tool. (qualitative measure)
up to 24 weeks
The mineralization status of the third molars
Time Frame: up to 24 weeks
the amount of calcified tissues of the third molar measured using Demirjian classification method
up to 24 weeks

Collaborators and Investigators

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

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)

September 4, 2021

Primary Completion (Actual)

June 4, 2023

Study Completion (Actual)

June 4, 2023

Study Registration Dates

First Submitted

September 8, 2021

First Submitted That Met QC Criteria

October 22, 2023

First Posted (Actual)

October 25, 2023

Study Record Updates

Last Update Posted (Actual)

October 25, 2023

Last Update Submitted That Met QC Criteria

October 22, 2023

Last Verified

October 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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