- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03225573
Prevalence of Second Mesiobuccal Canal of Maxillary First and Second Molars Among Egyptian Population (CBCT)
The Prevalence of a Second Mesiobuccal Canal of Maxillary First and Second Molars Using CBCT Among Egyptian Population: A Cross-Sectional Study
Study Overview
Status
Detailed Description
Setting and Location:
- The data collection will be obtained from the data base available at a private radiographic centre ORASCAN Oral & Maxillofacial Imaging Centre located in Cairo, Egypt.
- CBCT images will be obtained from Egyptian patients who had CBCT examination as part of their dental examination, diagnosis or treatment planning during the years 2015-16-17.
Participants:
A total of 196 CBCT scans of Maxillary first and second permanent molars belonging to Egyptian individuals will be included.
Variables:
- Number of root canals in mesiobuccal root of first and second maxillary molars
- Sex of the patient will be identified and addressed as the prevalence of the second mesiobuccal canal may show sex predilection
Data Sources / Measurements:
Retrospective Data Analysis will be performed after the CBCT images are pooled from the computer database.
All the CBCT examinations were scanned using Cranex® 3D SOREDEX, 0.2 voxel resolution, 8 × 6 cm FOV, 90 kVp, 10 mA and 6 seconds exposure time.
CBCT images will be analysed in the 3 planes; first the sagittal and coronal sections will be oriented parallel to the long axis of the root, and then sections will be obtained on the axial plane for detection of the 2nd mesiobuccal canal.
CBCT images will be interpreted by three oral radiologists independently; blinded from demographic data of the patients and from the results of each other.
Each one will evaluate the images separately twice with a period of two weeks between the two reading sessions.
Then inter-observational and intra-observational variability between the observers will be evaluated.
The sex of the patient will be identified from the patient's demographic data available on the patient's file on the database of the private radiographic centre.
Bias:
No source of bias.
Study Size:
The aim of the study is to assess the prevalence of a second mesiobuccal canal of maxillary first and second molars in Egyptian population. Based on the previous paper by Nikoloudaki et al, 2015, the prevalence of Second Mesiobuccal Canal of Maxillary First and Second Molars was 89 and 85%. Using a precision of 5, a design effect set at 1 with 95% CI (confidence interval), a total sample size of 196 will be sufficient. The sample size was calculated by Epi info.
Sampling Strategy: The sample will be collected by simple random sampling.
Quantitative Variables:
The number of CBCT scans of Egyptian individuals with second mesiobuccal canal will be counted to estimate the prevalence of the second mesiobuccal canal.
Statistical Methods:
- Data will be analysed using IBM SPSS advanced statistics (Statistical Package for Social Sciences), version 21 (SPSS Inc., Chicago, IL). Numerical data will be described as mean and standard deviation or median and range. Categorical data will be described as numbers and percentages. Comparisons between male and females for normally distributed numeric variables will be done using the Student's t-test while for non-normally distributed numeric variables will be done by Mann-Whitney test. Comparisons between categorical variables will be performed using the chi square test. A p-value less than or equal to 0.05 will be considered statistically significant. All tests will be two tailed.
- If the patient's age couldn't be found in the patient's file, the dental age will be used.
- If the patient's sex couldn't be found in the patient's file, the patient's name will be used to indicate the sex. Patients with mixed name will be excluded.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Maadi
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Cairo, Maadi, Egypt, 11728
- ORASCAN Oral and Maxillofacial Imaging Centre
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- First and second maxillary permanent molars of Egyptian patients starting from 15 years, males or females
- Intact roots without fractures or cracks
- Molars without posts or previous root canal treatment
- CBCT scans of maxillary first and second molars using 8 × 6 Field of view, 0.2 voxel resolution
Exclusion Criteria:
- Evidence of apicectomy or periapical surgery
- Odontogenic or non-odontogenic pathology
- Maxillary molars with developmental anomalies
- External or Internal Root resorption
- Canal Calcification
- Previous root canal treatment
- Extensive coronal restorations
- Posts or crown restorations
- Root caries specially reaching the trifurcation area
- Tomographic images of poor quality or artifacts interfering with the detection of root canals
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of Maxillary Molars With a Second Mesiobuccal Canal
Time Frame: 1 month
|
measuring device is CBCT software On Demand 3D® , measuring unit is binary system (yes/no)
|
1 month
|
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
Other Study ID Numbers
- Rad2:5:1
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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