Measurement of Mandibular Radio Morphometric Indices in Egyptian Population at Different Ages (Indices)

October 19, 2018 updated by: Hanaa Sayed Mansy, Cairo University

Measurement of Mandibular Radio Morphometric Indices in Egyptian Population at Different Ages Using Cone Beam Computed Tomography: A Cross Sectional Study

this study aims to correlate mandibular indices and different ages in a sample of Egyptian population.

Study Overview

Status

Unknown

Intervention / Treatment

Detailed Description

this study is an observational cross sectional study to correlate the mandibular radiomorphometric indices with age in sample of egyptian population using CBCT scans at faculty of dentistry cairo university

Study Type

Observational

Enrollment (Anticipated)

360

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, Egypt
        • Faculty of dentistry cairo univeristy

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

10 years to 70 years (Child, Adult, Older Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

a sample of egyptian population

Description

Inclusion Criteria:

  • Egyptian individuals with different ages starting from 10 - 70 years.
  • Females and males of the mentioned ages.

Exclusion Criteria:

  • Individuals younger than 10 and older than 70 years old.
  • Presence of a large pathological lesions in the mandible at the areas intended for measurements.
  • Patients of severely resorbed mandibular bone.
  • Patients with any bony deformity at the inferior border of the mandible.
  • Patients with fracture at the areas to be examined.
  • Patients with evident radiographic asymmetry.
  • Patients with evident radiographic abnormality suggestive of systemic disease predisposing to osteoporosis.
  • Patients with current postoperative surgical defect healing at the areas intended for measurements.
  • Patients with mandibular reconstruction

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
panoramic mandibular index
Time Frame: 2018-2020
ratio between the thickness of the mandible at the mental foramen area and the distance measured from the inferior border of the mental foramen to the inferior border of the mandible. The value of 0.3 will be considered as normal value while the lower value indicate abnormal inferior border thickness
2018-2020

Collaborators and Investigators

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

Investigators

  • Study Chair: Dentistry Cairo, Univeristy, Ethical committee faculty if dentustry cairo unveristry

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 (Anticipated)

October 30, 2018

Primary Completion (Anticipated)

June 1, 2019

Study Completion (Anticipated)

October 1, 2019

Study Registration Dates

First Submitted

October 18, 2018

First Submitted That Met QC Criteria

October 19, 2018

First Posted (Actual)

October 22, 2018

Study Record Updates

Last Update Posted (Actual)

October 22, 2018

Last Update Submitted That Met QC Criteria

October 19, 2018

Last Verified

October 1, 2018

More Information

Terms related to this study

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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