- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04543981
Prevalence of the Signs and Symptoms of TMD in Adolescents
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
Study Overview
Status
Conditions
Intervention / Treatment
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:
- palpation of TMJ area.
- digital palpation and functional manipulation of the masticatory muscles according to Okeson.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Mohamed Abdelaleem
- Phone Number: +2 01005246200
- Email: mohamed.abdelaleem@dentistry.cu.edu.eg
Study Contact Backup
- Name: Aya Abdelaleem, BDS
- Phone Number: +2 01012284977
- Email: ayaabdulrhman1993@gmail.com
Study Locations
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-
Cairo/Giza
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Cairo, Cairo/Giza, Egypt, 12511
- Recruiting
- Cairo University
-
Contact:
- Manal foda, professor
- Phone Number: 01006606864
- Email: manalyehia-3@hotmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
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
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
Sponsor
Investigators
- Study Director: Manal foda, professor, Cairo University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ORTH 1-1-1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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