- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03804437
The Prevalence and Anatomical Variations of Bifid Mandibular Canal in the Egyptian Population Using Cone Beam CT (CBCT)
The Prevalence and Anatomical Variations of Bifid Mandibular Canal in a Sample of Egyptian Population Using CBCT.A Hospital-based Cross-Sectional Study
Study Overview
Status
Conditions
Detailed Description
Settings:
The data collection will be obtained from the data base available at the department of Oral and Maxillofacial Radiology, Faculty of Dentistry, Cairo University. CBCT images will be obtained from Egyptian patients who were referred to the CBCT unit in oral and maxillofacial radiology department for different purposes.
Variables:
•Prevalence of bifid canals - Classification and prevalence of observed types - Distance from the involved teeth
Data Sources / Measurements:
- Retrospective Data Analysis will be performed after the CBCT images are pooled from the computer database.
- Exposure parameters of the scans will vary depending on patients' sizes (according to the manufacturer's recommendations).
- Both images with 0.2 and 0.4 voxel sizes will be reviewed.
- For proper visualization of the mandibular canal, the reference lines will be rotated, so that it lies perpendicular to the mandibular foramen on the axial cuts. Then, scrolling through the corrected sagittal cuts will be performed to review the clearest cut of the full course of the mandibular canal. Moreover, corrected coronal cuts will be reviewed, to determine the exits of the accessory branches (buccal or lingual) if present.
- CBCT images will be interpreted by two oral and maxillofacial radiologists (with different experiences) independently; blinded from demographic data of the patients and from the results of each other.
The classification of Naitoh et al 2009 will be followed for the categorization of the accessory branches:
- Forward canal: emerging from the superior wall of the main canal.
- Bucco-lingual canal: emerging from the buccal or the lingual wall of the main canal.
- Dental canal: the end of the bifid canal is at the root apex of the molars.
- Retromolar canal: emerging from the main canal, opening at the retromolar foramen in the retromolar area.
- Each radiologist will evaluate the images for presence of bifid canal twice with a time lag of two weeks between the two reading sessions. If present, its configuration (classification) will be registered. Any disagreement will be solved by consensus between the two observers.
- If adherence or closeness of the canals to the teeth is detected, then the distance between the canal and the involved tooth will be measured using built in measuring tool in the software.
- The measurements will be carried out by one observer (EE) and will be repeated 2 weeks later for intra-observer reliability assessment.
Bias
No source of bias.
Study Size:
The aim of the study is to assess the prevalence of bifid mandibular canal in Egyptian population. Based on the previous paper by Afsa and Rahmati 2017, the prevalence of bifid mandibular canal was 31% Using a precision of 5, a design effect set at 1 with 95% CI (confidence interval), a total sample size of 329 hemimandibles will be sufficient. The sample size was calculated by Epi info 7 software.
Quantitative Variables:
Quantitative data: The distance between the canal and involved teeth and will be reported as mean and standard deviation.
Statistical methods:
Data will be analyzed using SPSS® v. 15 (SPSS Inc., Chicago, IL) software program. Pearson Chi square and t-tests was performed for statistical analysis among gender, localization and measurements. Categorical data will be described as numbers and percentages. A p value of <0.05 will be considered statistically significant.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Cairo, Egypt
- Faculty of Dentistry, Cairo University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Age range from 18 to 70
- Scans showing the premolar, molar, retromolar areas.
Exclusion Criteria:
- Patients with mandibular lesions.
- Scans with severe metallic artifacts.
- Patients with previous fractures or surgeries.
- Severe bone resorption.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Bifid mandibular canal detection, measuring device is CBCT software Romexis, measuring unit is percentage ( Dichotomous data - Yes or No )
Time Frame: up to 2019
|
Detection of bifid mandibular canal in Egyptian population
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up to 2019
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Prevalence of types,measuring device is CBCT software Romexis, measuring unit is Categorical nominal data(%)
Time Frame: up to 2019
|
They are either Forward canal, Bucco-lingual canal , Retromolar canal, Dental canal
|
up to 2019
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Distance to adjacent teeth, measuring device is Built-in measuring tool (ruler), measuring unit is mm
Time Frame: up to 2019
|
distance to adjacent teeth will be measured
|
up to 2019
|
Region of exit of retromolar canal,measuring device is CBCT software Romexis, measuring unit is Categorical nominal data (%)
Time Frame: up to 2019
|
They are either buccal or lingual or non-visible
|
up to 2019
|
Prevalence according to gender,measuring unit is categorical nominal data (%)
Time Frame: up to 2019
|
They are either male or female
|
up to 2019
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
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
Keywords
Other Study ID Numbers
- ORAD 7-1-1
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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