- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07341906
Diagnosis Evaluation Made by Artificial Inteligence in Response to a Request Made by General Praticioner on OMNIDOC to the Dermatologist of the CHU of Nice. A Comparison of This Response by the One Made by the Dermatologist.
Evaluation of the Contribution of Artificiel Inteligence on a Dermatologist Tele -Expertise Request Made by General Praticioner : a Retrospective and Single-center Study.
The First part of the study will be the inclusion of our patients (those for whom a tele-expertise request has been made by their general practitioner on the OMNIDOC platform between the 1st of May 2024 and the 31st of December 2025. ) After that, the team will investigate the non opposition patient to the use of their personal information.
Subsequently, the clinical study will focus on comparing the diagnosis made by chat gpt expert and a dermatologist from the University Hospital of Nice to a request of dermatology tele-expertise made by general praticioner on OMNIDOC
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
-
-
Alpes Maritimes
-
Nice, Alpes Maritimes, France, 06000
- Chu de Nice
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adult with a request on OMNIDOC made by their general practitioner.
- Adult not opposed Social Security affiliation.
- Diagnosis made by a dermatologist.
Exclusion Criteria:
- Pediatric case.
- Unusable image.
- Absence of diagnosis made by a dermatologist.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Expert opinion
The expert had provided a diagnosis and a support based on the guideline in France
|
The expert had provided a diagnosis and a support based on the guideline in France
|
|
chatGPT opinion
ChatGPT will provide a diagnosis and the support based on the guideline in France
|
The expert had provided a diagnosis and a support based on the guideline in France
|
|
Specialized AI opinion
Specialised IA will provide a diagnosis and the support based on the guideline in France
|
The expert had provided a diagnosis and a support based on the guideline in France
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Compare the diagnoses offered by artificial intelligence to those proposed by the experts on requests for tele-expertise.
Time Frame: From 01 May 2025 - 31 December 2026
|
Check the correspondence between the diagnosis made by the expert and the artificial intelligence on the photos, the diagnosis and supports.
|
From 01 May 2025 - 31 December 2026
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Compare the support and response times offered by artificial intelligence to those offered by experts for dermatology tele-expertise requests.
Time Frame: From 01 May 2025 - 31 December 2026
|
Check the consistency between the expert's instructions and the timeframe for intervention, and the information provided by the two artifical intelligence by The photos, the diagnosis and supports
|
From 01 May 2025 - 31 December 2026
|
|
Compare the differences between the responses offered by chatGPT and the specific dermatologic artificial intelligence
Time Frame: From 01 May 2025 - 31 December 2026
|
Compare the differences between the responses offered by chatGPT and the specific dermatologic artificial intelligence by the photos, the diagnosis and supports
|
From 01 May 2025 - 31 December 2026
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 25MedInterne01
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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