- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03175445
Sexual Dimorphism Analysis in Egyptian Population by Locating the Mandibular Canal Using CBCT
June 1, 2017 updated by: Arwa Mousa, Cairo University
Sexual Dimorphism Analysis in Egyptian Population by Locating the Mandibular Canal Using Cone-beam Computed Tomography: an Observational Cross Sectional Study
Sexual dimorphism analysis in Egyptian population by locating the mandibular canal using cone-beam computed tomography: an observational cross sectional study
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed 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.
Study Type
Observational
Enrollment (Actual)
136
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
-
-
-
Cairo, Egypt
- Cairo University
-
-
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
18 years to 88 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Adult Egyptian population
Description
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.
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
mandible CBCT scans in males
74 males CBCT scan by planmeca promax 3D Mid machine using 90 kVp, 10 mA, 14 seconds and 200×60 mm FOV with a 0.2 mm voxel size.
|
software measurement tool of CBCT
|
mandible CBCT scans in female
74 females CBCT scan by planmeca promax 3D Mid machine using 90 kVp, 10 mA, 14 seconds and 200×60 mm FOV with a 0.2 mm voxel size
|
software measurement tool of CBCT
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Anterior ramus width , posterior ramus width
Time Frame: 2 years
|
distance from mandibular foramen to most anterior and posterior points of ramus respectively
|
2 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Arwa Mousa, 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)
January 30, 2017
Primary Completion (Anticipated)
December 30, 2017
Study Completion (Anticipated)
January 1, 2019
Study Registration Dates
First Submitted
May 30, 2017
First Submitted That Met QC Criteria
June 1, 2017
First Posted (Actual)
June 5, 2017
Study Record Updates
Last Update Posted (Actual)
June 5, 2017
Last Update Submitted That Met QC Criteria
June 1, 2017
Last Verified
June 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- CEBD-CU-2017-05-09
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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