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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05987215
Other study ID # 22-5019 / 69HCL22_1193
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date July 1, 2022
Est. completion date October 1, 2023

Study information

Verified date May 2023
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Otosclerosis is a relatively frequent pathology, of multifactorial origin with genetic and hormonal part, predominantly in women. This disease causes a disorder of the bone metabolism of the middle and inner ear, responsible for a progressive deafness, which can become severe. Several elements are necessary to make the diagnosis of otosclerosis: the clinical examination and questioning, the audiometric assessment, and finally the temporal bone CT. The CT scan allows to detect foci of otosclerosis within the bone of the middle or inner ear. This diagnosis is sometimes difficult and requires interpretation by a trained radiologist. The investigators would like to evaluate the ability of a deep learning algorithm to detect these foci of otosclerosis, and to compare its diagnostic performance with a trained radiologist.


Description:

Otosclerosis is a relatively frequent pathology, of multifactorial origin with genetic and hormonal part, predominantly in women. This disease causes a disorder of the bone metabolism of the middle and inner ear, responsible for a progressive deafness, which can become severe. Several elements are necessary to make the diagnosis of otosclerosis: the clinical examination and questioning, the audiometric assessment, and finally the temporal bone CT. The CT scan allows to detect foci of otosclerosis within the bone of the middle or inner ear. This diagnosis is sometimes difficult and requires interpretation by a trained radiologist. The investigators would like to evaluate the ability of a deep learning algorithm to detect these foci of otosclerosis, and to compare its diagnostic performance with a trained radiologist.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 240
Est. completion date October 1, 2023
Est. primary completion date May 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 110 Years
Eligibility - Inclusion Criteria * : - age over 18 - high resolution temporal bone CT scan available for analysis - for the "case" group : surgical confirmation of positive diagnosis for otosclerosis - for the "control" group : a first radiological analysis in favor of a normal temporal bone CT scanner and an initial radiologic report considered normal as well - Exclusion Criteria * : - age under 18 - no high resolution temporal bone CT scan available for analysis - unwillingness to participate in the study

Study Design


Related Conditions & MeSH terms


Intervention

Combination Product:
Radiologic diagnosis
Each CT scan is interpreted by a radiologist and is assigned as positive or negative for the diagnosis of otosclerosis
Diagnostic Test:
Artificial intelligence diagnosis
Each CT scan is screened by the deep learning algorithm and is assigned as positive or negative for the diagnosis of otosclerosis

Locations

Country Name City State
France Hospices Civils de Lyon, Centre Hospitalier Lyon sud, Service d'ORL, d'otoneurchirurgie et de chirurgie cervico-facaile Pierre-Bénite

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Diagnostic performance of the artificial intelligence algorithm compared to the diagnostic performance of the radiologist : sensitivity, specificity, positive and negative predictive value, area under the ROC curve These diagnostic performances will be established from the positive or negative diagnoses of the algorithm and the radiologist, compared to the "case" or "control" status of each patient included in the study through study completion, an average of 5 months
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