Analysis of Adverse Events in Anesthesia Using Artificial Intelligence

NCT ID: NCT05185479

Last Updated: 2023-12-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

9559 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-11-12

Study Completion Date

2021-11-12

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The interest of health databases in anesthesia is no longer to be demonstrated. The aim of this research was to develop a natural language processing approach to establish a classification of adverse events observed during the perioperative period and to facilitate their analysis:

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

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Allergic Reaction

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Allergic Reaction Adverse events Health database Natural Language Processing

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Minors and adults having had an allergic reaction associated with care
* Having had an adverse event reported by an anesthetist between January 01, 2009 and June 30, 2020
Minimum Eligible Age

1 Year

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University Hospital, Strasbourg, France

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Paul-Michel MERTES, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Service d'Anesthésie et Réanimation chirurgicale - CHU de Strasbourg - France

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Service d'Anesthésie et Réanimation chirurgicale - CHU de Strasbourg - France

Strasbourg, , France

Site Status

Countries

Review the countries where the study has at least one active or historical site.

France

References

Explore related publications, articles, or registry entries linked to this study.

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.

Reference Type DERIVED
PMID: 38718923 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

8505

Identifier Type: -

Identifier Source: org_study_id