- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06164184
Interest of the Cone Beam Scanner of Temporal Bones in the Analysis of Conductive Hearing Loss (Cone-Beam)
Conductive hearing loss is very common and the incidence increases with age. Until now, the scanner was the reference examination in the etiological diagnosis of deafness.
When performing a CT scan of temporal bones for the etiological diagnosis of conductive hearing loss, the quality of the image depends on the scanner brand and the acquisition parameters.
The investigators wish to show the usefulness of the cone beam in the diagnosis of conductive hearing loss
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: francis VEILLON, MD, PhD
- Phone Number: 33 3 88 12 78 65
- Email: francis.veillon@chru-strasbourg.fr
Study Locations
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Strasbourg, France, 67091
- Recruiting
- Service de Radiologie 1 - CHU de Strasbourg - France
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Sub-Investigator:
- Julien UTTNER, MD
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Contact:
- francis VEILLON, MD, PhD
- Phone Number: 33 3 88 12 78 65
- Email: francis.veillon@chru-strasbourg.fr
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Principal Investigator:
- Francis VEILLON, MD, PhD
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Major subject (≥18 years old)
- Subject having performed a CT scan or a cone beam for pre- and post-operative conductive hearing loss between January 01, 2018 and December 31, 2020
- Subject who has not expressed his opposition, after being informed, to the reuse of his data for the purposes of this research.
Exclusion Criteria:
- Subject who expressed their opposition to participating in the study
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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Show retrospectively that the superiority of the cone beam over the scanner in the diagnosis of conductive hearing loss
Time Frame: Files analysed retrospectively from January 01, 2018 to December 31, 2020 will be examined
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This superiority is based on the quality of the images allowing the visualization of the different elements of the middle and inner ears: Ossicles, windows, nerves (VII and VIII), cochlea, labyrinth |
Files analysed retrospectively from January 01, 2018 to December 31, 2020 will be examined
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Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 8012 (Oregon Health & Science University)
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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