Evaluation of Treatment Outcomes With Palatal Plate Versus Conventional Tooth Borne Anchorage in Class III Patients

January 16, 2026 updated by: Yousra Mohamed Saad, Faculty of Dental Medicine for Girls
evaluation of treatment outcomes with palatal plate versus conventional tooth borne anchorage in class III patients

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

group (A) patients were treated with transpalatal arch and facemask. group(B) patients were treated by palatal plate and facemask

Study Type

Interventional

Enrollment (Actual)

14

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

  • Egypt
      • Cairo, Egypt
        • Faculty of Dentistry , Al Azhar University, Girls Branch, Cairo

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

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • skeletal class III malocclusion deficient maxilla+ growing patient

Exclusion Criteria:

  • adult patient, cleft patient

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: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: treatment of skeletal class III by maxillary advancement using transpalatal arch
treatment of skeletal class III by maxillary advancement, using transpalatal arch and facemask
Device: treatment of skeletal class III by maxillary advancement using transpalatal arch and face mask
TPA group
Experimental: treatment of skeletal class III by maxillary advancement by skeletal anchorage
treatment of skeletal class III by maxillary advancement by skeletal anchorage using palatal plate and face mask
Device: treatment of skeletal class III by maxillary advancement using palatal plate and face mask
palatal plate group

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
skeletal and dental maxillary changes including SN angle, SNB angle, ANB angle
Time Frame: 3-12 months
lateral cephalometry
3-12 months

Collaborators and Investigators

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

Sponsor

Faculty of Dental Medicine for Girls

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Helpful Links

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)

August 15, 2023

Primary Completion (Actual)

September 30, 2025

Study Completion (Actual)

November 11, 2025

Study Registration Dates

First Submitted

January 10, 2026

First Submitted That Met QC Criteria

January 16, 2026

First Posted (Actual)

January 22, 2026

Study Record Updates

Last Update Posted (Actual)

January 22, 2026

Last Update Submitted That Met QC Criteria

January 16, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • ORTHO-109-3-G

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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