Analysis of Adverse Events in Anesthesia Using Artificial Intelligence
NCT ID: NCT05185479
Last Updated: 2023-12-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
9559 participants
OBSERVATIONAL
2020-11-12
2021-11-12
Brief Summary
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The main objective of the study was to identify what a "naïve" unsupervised model would discover based on Adverse Event (AE) descriptions. Our second goal was to identify apparently unrelated events whose combination could favor the occurrence of an AE
Detailed Description
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Conditions
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Keywords
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Study Design
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CASE_ONLY
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Having had an adverse event reported by an anesthetist between January 01, 2009 and June 30, 2020
1 Year
ALL
No
Sponsors
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University Hospital, Strasbourg, France
OTHER
Responsible Party
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Principal Investigators
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Paul-Michel MERTES, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Service d'Anesthésie et Réanimation chirurgicale - CHU de Strasbourg - France
Locations
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Service d'Anesthésie et Réanimation chirurgicale - CHU de Strasbourg - France
Strasbourg, , France
Countries
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References
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Mertes PM, Morgand C, Barach P, Jurkolow G, Assmann KE, Dufetelle E, Susplugas V, Alauddin B, Yavordios PG, Tourres J, Dumeix JM, Capdevila X. Validation of a natural language processing algorithm using national reporting data to improve identification of anesthesia-related ADVerse evENTs: The "ADVENTURE" study. Anaesth Crit Care Pain Med. 2024 Aug;43(4):101390. doi: 10.1016/j.accpm.2024.101390. Epub 2024 May 6.
Other Identifiers
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8505
Identifier Type: -
Identifier Source: org_study_id