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OpenTrials
Completed

NCT Number: NCT05076188

PARamedical Abnormalties Detection of Traumatic Bone Lesion of the extremitIeS

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.

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Key information

Conditions

Radiography Diagnostic Disease Disease Attributes Emergencies Pathologic Processes Pathological Conditions, Signs and Symptoms

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Observational

Primary location

C.H.U. de Poitiers

Poitiers, 86000, France

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Working in an emergency radiography department Volunteer to participate in the study

Exclusion criteria

  • Planned departure from the establishment within 12 months.

Treatment and study plan

Emergency radiography

Diagnostic Test

The intervention is to determine how the radiographer classify emergency radiography.

Primary outcomes

  1. Evaluate the radiographers' diagnostic performance to issue an advisory opinion to X-ray reading of the appendicular skeleton in emergency department

    Time frame: 2 hours

    The primary outcome measure evaluation radiographers' diagnostic will use accurancy, sensibility and specificity.

Secondary outcomes

  1. Quantify the proportion of radiographers reaching the goal of 90% accurancy

    Time frame: 4 months

    This is a proportion in % of performance radiographers' diagnosctic treshold

  2. Quantify and qualify Radiographers diagnostic changes before and after the in house training.

    Time frame: 4 months

    This a proportion in % about the progression of performance radiographers'diagnostic in the formation.

  3. Evaluate the performance of the association of AI and radiographer after training

    Time frame: 4 months

    Thiis output is the difference between accurancy, sensibility and sensitivity with or without IA.

Sponsors and collaborators

Lead sponsor

Poitiers University Hospital

Other

Registry information

Acronym: PARADIS_1

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Oct 13, 2021
Registry last updated
Nov 2, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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