Prevalence of the Signs and Symptoms of TMD in Adolescents

September 3, 2020 updated by: Mohamed Abdelrahman Abdelaleem, Cairo University

Prevalence of the Signs and Symptoms of Tempro-mandibular Joint Disorder in a Sample of Egyptian Adolescents According to Diagnostic Criteria for Tempro-mandibular Disorders(DC/TMD):A Cross Sectional Study

the Prevalence of the Signs and Symptoms of Tempro-mandibular Joint Disorder in a sample of Egyptian adolescents

Study Overview

Detailed Description

Our study is observational cross sectional study to evaluate the prevalence ofTempro-mandibular Joint Disorder( TMDs) in Egyptian adolescents based on Diagnostic Criteria for Tempro-mandibular Disorders(DC/TMD) .The following examinationwill be done for each patient and recorded in his/her chart:

Include maximal mandibular opening capacity, joint noises, deviation of mandible during opening and closing, tenderness of the TMJ and masticatory muscles, headache and pain in TMJ area.

All clinical examinations will be carried out by one investigator. Examination of TMJ disorders include the following aspects: I) Examination of TMJ sounds (clicking and crepitus) using a stethoscope over the TMJ area and by having the patient open and close the mouth.

II) Associated muscle disorders will be determined by:

  1. palpation of TMJ area.
  2. digital palpation and functional manipulation of the masticatory muscles according to Okeson.

Study Type

Observational

Enrollment (Anticipated)

733

Contacts and Locations

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

Study Contact

Study Contact Backup

Study Locations

    • Cairo/Giza
      • Cairo, Cairo/Giza, Egypt, 12511

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

8 years to 16 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

DC/TMD shhts will be assessed and obtained from adolescents in Diagnostic center clinic at the faculty of Dentistry, Cairo University

Description

Inclusion Criteria:

  • Adolescents(age range10-18 years old).
  • A well-defined dentalCl I, Cl II/1, Cl II/2, and Cl III relationship (Angle Classification).
  • Mixed and permanent dentition.
  • Both sexes.
  • Normal skeletal pattern

Exclusion Criteria:

  • Adolescents with syndromes.
  • Systemic diseases affecting bones.
  • Adolescents with rheumatoid arthritis.
  • Previous trauma in the face.
  • Neurological disorders.
  • Psychiatric disorders.
  • Neoplasia.
  • Adolescents who had received orthodontic treatment.

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

  • Observational Models: Cohort
  • Time Perspectives: Cross-Sectional

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
TMD
Time Frame: at the time of examination of each participant
adolescents diagnosed positively for any TMD subtype (overall TMD) by DC/TMD.
at the time of examination of each participant

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Myofacial pain
Time Frame: at the time of examination of each participant
pain in each muscle of mastication will be recorded
at the time of examination of each participant
mouth opening
Time Frame: at the time of examination of each participant
limitation of mouth opening and pain during such movement
at the time of examination of each participant
TMJ noises
Time Frame: at the time of examination of each participant
Clicking and crepitus in tempro-mandibular joint
at the time of examination of each participant

Collaborators and Investigators

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

Investigators

  • Study Director: Manal foda, professor, Cairo 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)

July 1, 2020

Primary Completion (Anticipated)

June 1, 2021

Study Completion (Anticipated)

July 1, 2021

Study Registration Dates

First Submitted

September 3, 2020

First Submitted That Met QC Criteria

September 3, 2020

First Posted (Actual)

September 10, 2020

Study Record Updates

Last Update Posted (Actual)

September 10, 2020

Last Update Submitted That Met QC Criteria

September 3, 2020

Last Verified

September 1, 2020

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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