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NCT05076188 Clinical Trial

PARamedical Abnormalties Detection of Traumatic Bone Lesion of the extremitIeS

Emergencies Clinical Trial

— PARADIS_1  

Official title:
PARamedical Abnormalties Detection of Traumatic Bone Lesion of the extremitIeS

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05076188
Other study ID # Paradis_1
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 1, 2021
Est. completion date September 1, 2021

Study information
Verified date March 2021
Source Poitiers University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study assesses the performance of radiographers in detecting radiological anomalies of the appendicular skeleton in emergency department. This is a retrospective study comparing the radiographers' diagnostic performance before and after dedicated training, assisted or not by artificial intelligence software. All performances will be evaluated and compared.

Recruitment information / eligibility
Status Completed
Enrollment 19
Est. completion date September 1, 2021
Est. primary completion date July 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - Working in an emergency radiography department Volunteer to participate in the study Exclusion Criteria: - Planned departure from the establishment within 12 months.

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• Emergency radiography
The intervention is to determine how the radiographer classify emergency radiography.

Locations
Country Name City State
France C.H.U. de Poitiers Poitiers

Sponsors (1)
Lead Sponsor Collaborator
Poitiers University Hospital

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Evaluate the radiographers' diagnostic performance to issue an advisory opinion to X-ray reading of the appendicular skeleton in emergency department The primary outcome measure evaluation radiographers' diagnostic will use accurancy, sensibility and specificity. 2 hours
Secondary Quantify the proportion of radiographers reaching the goal of 90% accurancy This is a proportion in % of performance radiographers' diagnosctic treshold 4 months
Secondary Quantify and qualify Radiographers diagnostic changes before and after the in house training. This a proportion in % about the progression of performance radiographers'diagnostic in the formation. 4 months
Secondary Evaluate the performance of the association of AI and radiographer after training Thiis output is the difference between accurancy, sensibility and sensitivity with or without IA. 4 months
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