Sexual Dimorphism Analysis in Egyptian Population by Locating the Mandibular Canal Using CBCT

Gender Identity Clinical Trial

Official title:

Sexual Dimorphism Analysis in Egyptian Population by Locating the Mandibular Canal Using Cone-beam Computed Tomography: an Observational Cross Sectional Study

Clinical Trial Details — Status: Enrolling by invitation

Administrative data

• NCT number: NCT03175445
• Other study ID #: CEBD-CU-2017-05-09
• Status: Enrolling by invitation
• Phase: N/A
• First received: May 30, 2017
• Last updated: June 1, 2017
• Start date: January 30, 2017
• Est. completion date: January 1, 2019

Study information

• Verified date: June 2017
• Source: Cairo University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Sexual dimorphism analysis in Egyptian population by locating the mandibular canal using cone-beam computed tomography: an observational cross sectional study

Description:

Many studies from different countries such as United States, China, Japan, and Europe were done to observe the distinct morphologic and morphometric manifestations of sexual dimorphism. Accordingly, it is mandatory to target a specific population with their unique skeletal features.

Recruitment information / eligibility

• Status: Enrolling by invitation
• Enrollment: 136
• Est. completion date: January 1, 2019
• Est. primary completion date: December 30, 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 88 Years

Eligibility

Inclusion Criteria:

• 18 years and above.

• Absence of large pathological lesions in mandible.

• Dentulous patients

Exclusion Criteria:

• Patients younger than 18 years old

• Presence of large pathological lesions in mandible

• Completely edentulous patients.

Related Conditions & MeSH terms

• Gender Identity

Intervention

Other:
• CBCT scan by planmeca promax
software measurement tool of CBCT

Locations

Country	Name	City	State
Egypt	Cairo university	Cairo

Sponsors (1)

Lead Sponsor	Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Anterior ramus width , posterior ramus width	distance from mandibular foramen to most anterior and posterior points of ramus respectively	2 years