- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06765148
Radiodiagnostic Properties of Maxillary Antroliths
Radiodiagnostic Properties of Maxillary Antroliths: a Retrospective Cone Beam Computed Tomography Study
Background: To evaluate the frequency and radiodiagnostic characteristics of maxillary antroliths using cone beam computed tomography.
Materials and Methods: A review of 1166 patients aged 11-85 years was conducted to assess the frequency of maxillary antroliths, considering sex, age, and location. The relationship between antroliths and sex, location, dental treatment status, and sinus inflammation was evaluated. The shape, size, and volume of the antroliths were also analyzed. Significance was set at p=0.05 for statistical analysis.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Rize, Turkey, 53100
- Recep Tayyip Erdogan University Training and Research Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- DPR and CBCT and also had a maximum of 3 months
- Image quality was sufficient
- No artifacts CBCT images
Exclusion Criteria:
- Tomographic images that contained pathologies such as cysts/tumors in the
- Insufficient diagnostic quality
- History of maxillofacial trauma or surgery, any syndrome/bone-related disease/metabolic disease
- Insufficient diagnostic quality or patient position-related artifacts
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Antrolith descriptive analysis
Time Frame: for three days from the beginning of the study
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CBCT images were examined in axial, sagittal, and coronal slices to investigate the presence of antroliths.
The age and sex information of the detected cases were recorded.
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for three days from the beginning of the study
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Antrolith localization and relationship the dental status evaluation
Time Frame: for three days from the beginning of the study
|
Each sinus cavity exhibiting antroliths was evaluated for distribution and location as follows: (1) unilateral or bilateral, (2) single or multiple, (3) tooth extraction/root canal treatment/residual root fragment/implant/periodontal disease and/or periapical lesion (any dental cause of sinus inflammation), (4) premolar or molar region, and (5) sinus floor, lateral wall, or medial wall.
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for three days from the beginning of the study
|
|
Antrolith and mucosal thickness classification
Time Frame: for three days from the beginning of the study
|
the detected antroliths were categorized according to the classification of Cho et al. In this classification made according to the sizes of antroliths, Punctate = ≤3 mm in both height and width, Linear = ≤3 mm and more than treble in width, and Amorphous = >3 mm in both width and height. Additionally, the locations of the openings of the maxillary sinus ostiums were evaluated, and mucosal thickening, if any, was measured. Mucosal thickness measurements were made on coronal slices using NewTom's NNT viewer measuring tool. Similar to Chen et al., the sinus membrane thickness was measured perpendicular to the bone wall, from the maximum thickest region. Similar to Chen et al.'s classification of sinus membrane thickness measurements, which used Block and Dostoury's classification, the mucosal thickness was classified into three subgroups: membrane thicknesses <2 mm, 2-5 mm, and >5 mm. Also, similar to the article by Cho et al., the degree of inflammation in the maxillary sinus was |
for three days from the beginning of the study
|
|
Antrolith volume measurement
Time Frame: for three days from the beginning of the study
|
3D reconstruction and volume measurements of antroliths were performed using the ITK SNAP software (free software under the GNU General Public License developed by the National Institutes of Health, the US National Institute of Biomedical Imaging and Bioenergy needs, the US National Library of Medicine, the Universities of Pennsylvania and North Carolina, and an independent group of developers).
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for three days from the beginning of the study
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Different images evaluation for antrolit
Time Frame: for three days from the beginning of the study
|
In addition, the visibility of antroliths detected on CBCT was also evaluated using panoramic radiographs taken from the patient (Fig 2).
The detectability of antroliths in DPRs was evaluated by observers as detectable, suspicious, and undetectable.
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for three days from the beginning of the study
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Collaborators and Investigators
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
- 2024/299
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
product manufactured in and exported from the U.S.
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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