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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06306599
Other study ID # Thyroid AI US operator exp
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2023
Est. completion date November 4, 2023

Study information

Verified date March 2024
Source Rigshospitalet, Denmark
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a prospective clinical study aiming to test how the experience of the ultrasound operator influences the performance of AI-based (artificial intelligence-based) diagnostics when analysing thyroid nodules on ultrasound scans. The investigators set up an experiment with five stations, each with a patient with a thyroid nodule and an ultrasound machine with the deep learning based system S-Detect for Thyroid installed. 20 study participants where recruited: 8 medical students of novice ultrasound skill, 3 junior ENT (ear-nose-throat) registrars of intermediate ultrasound skill, and 9 senior ENT registrars experienced in ultrasound. The participants scanned all the patients and recorded their analyses of the nodules using the EUTIRADS (European thyroid imagining reporting and data system) system in three different ways: a analysis of their own, S-Detect's analysis, and an analysis combining the two previous. The hypothesis was that the AI system would perform equally well when between the participant groups. In addition, it was expected that the experienced participants would perform better than the students without AI help, and that the doctors would gain little from AI input, but that the students would have their performance improved by AI input.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date November 4, 2023
Est. primary completion date November 4, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Medical students Inclusion Criteria: - Last year student Exclusion Criteria: - Experience with ultrasound beyond that which is taught at the University of Copenhagen Junior ENT registrar doctors Inclusion Criteria: - Doctor enrolled in introductory training as ENT physician. Senior ENT registrar doctors Inclusion Criteria: - Doctor enrolled in ENT training.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
S-Detect for Thyroid
Deep learning based program on Samsung ultrasound machines designed to do real-time semi-automated analysis of thyroid nodules. The ultrasound operator freezes a transverse image of the patient's thyroid nodule and activates S-Detect. The operator selects the nodule on the screen, and the program automatically draws a region of interest. Then S-Detect gives a dichotomous diagnosis of either "Possibly benign" and "Possibly malignant". In addition, it measures the nodule and characterises it with a lexicon based on EUTIRADS.

Locations

Country Name City State
Denmark Rigshospitalet Copenhagen

Sponsors (1)

Lead Sponsor Collaborator
Rigshospitalet, Denmark

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Accuracy of S-Detect diagnosis Number of correct thyroid nodule malignancy diagnoses out of total malignancy diagnoses by the AI-based ultrasound diagnostic system "S-Detect" on the five patients' thyroid nodules. Gold standard is cytology and histology of the nodules. 1 day (day of experiment)
Secondary Accuracy of biopsy recommendation Number of correct biopsy recommendations on the five patients' thyroid nodules. Recommendation is derived from EUTIRADS analyses done by participants with and without AI assistance. Gold standard is biopsy recommendation derived from expert consensus EUTIRADS assessment of the nodules. 1 day (day of experiment)
Secondary Nodule classification agreement Agreement of nodule classification with gold standard. Nodule classifications are derived from EUTIRADS done by participants, S-Detect, and participant with S-Detect input on the five patients' thyroid nodules. Gold standard is expert consensus EUTIRADS assessment of the nodules. 1 day (day of experiment)
Secondary Accuracy of EUTIRADS scores Number of correct EUTIRADS scores given by analyses from participants, S-Detect, and participants with S-Detect input on the five patients' thyroid nodules. Gold standard is EUTIRADS score from expert consensus EUTIRADS assessment of the nodules. 1 day (day of experiment)
Secondary Nodule measurement Measurement of the five patients' thyroid nodules done by participants and S-Detect. Gold standard are measurements from expert consensus assessment analysis of the nodules. 1 day (day of experiment)
Secondary OSAUS score Mean OSAUS (objective structured assessment of ultrasound skills) scores of participants as assessed from their ultrasound scans of the five patients. Assessment are independently by two head-and-neck ultrasound experts. 1 day (day of experiment)
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