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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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23 March 2015 |
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Main ID: |
NCT02121236 |
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Date of registration:
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21/04/2014 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Diagnostic Accuracy of Ultrasonography in Detecting Benign Radiolucent Lesions
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Scientific title:
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Diagnostic Accuracy of Ultrasonography in Detecting Benign Radiolucent Lesions Compared to CBCT Imaging and Histological Examination |
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Date of first enrolment:
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April 2014 |
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Target sample size:
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25 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT02121236 |
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Study type:
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Observational |
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Study design:
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Observational Model: Case-Only, Time Perspective: Cross-Sectional
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Phase:
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N/A
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Countries of recruitment
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Syrian Arab Republic
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Contacts
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Name:
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Iyad Al-Haffar, DDS MSc Phd |
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Address:
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Telephone:
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Email:
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Affiliation:
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Associate Professor of Oral Medicine, Department of Oral Medicine, University of Damascus Dental School, Damascus |
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Name:
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Obai Zainedeen, DDS MSc |
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Address:
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Telephone:
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Email:
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Affiliation:
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PhD student, Department of Oral Medicine, University of Damascus Dental School, Damascus |
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Name:
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Nabeel Kushaji, DDS MSc PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Associate Professor of Oral Medicine, Department of Oral Medicine, University of Damascus Dental School |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- the presence of a radiolucent or mixed-appearance intraosseous lesion in the upper
or lower jaw requiring surgical removal
- no previous trauma to the maxillofacial region.
- no previous surgical intervention in the same area of the lesion.
Exclusion Criteria:
- the presence of a completely radiopaque lesion indicating solid content.
- patients with systemic conditions associated with bony pathology such as
hyperparathyroidism, Paget disease, ?brous dysplasia, multiple myeloma, etc...
Age minimum:
20 Years
Age maximum:
50 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Benign Radiolucent Lesions
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Primary Outcome(s)
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Lesion Contents
[Time Frame: One time assessment once sample recruitment has completed. Ultrasonographic images will be taken before the surgical intervention of the lesion, whereas the histological examination will be performed after the surgical removal]
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Secondary Outcome(s)
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3D measurements of the lesion
[Time Frame: One time assessment once sample recruitment has completed.]
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Secondary ID(s)
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UDDS-OraMed-02-2014
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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