Ireland
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Recruiting Observational

Morbidity and Mortality: Surgery and Standardized Transmission in Operating Room

NCT05440331 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2023-09-08
Last updated
2025-11-19

Condition(s) studied

Major Surgery

Investigational drug(s) / intervention(s)

Training with AnesList©

Training with AnesList©: Training with AnesList© as tool

Study summary

The primary objective of the study is to evaluate the efficacy of standard handover with AnesList© between physician anesthesists in operating room, for a complete transmission for a patient, on the occurence of event as death, serious complications or rehospitalization in month of postoperative after major surgery.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patient aged \> 18 years; * Patients with score ASA I-IV; * Requiring urgent or planned surgery; * Major surgery (duration of surgery \> 2 hours, requiring a hospital stay of at least 1 night): orthopedics, cardiac, vascular, thoracic, visceral, ENT, plastic surgery; * Handover between two anesthesists defined as a definitive relay between one physician anaesthesist and another in operating room; * Intensive care anesthesists and nurse anaesthetist working in investigator center during the study; * Affiliated to a social security system; * No-opposition to participating to the study. Exclusion Criteria: * Transmission between physician anaesthesist and nurse anaesthetist; * Medical transmission occurs out of anesthesia care out of operating room; * Medical transmission occurs in transitory manner (for example: coffee time, lunch time); * Patients enrolled in an another ongoing study of surgical intervention.

Primary outcome measure(s)

  • The occurence of adverse events — at 1 month
    Death, serious complications and re-hospitalization will be noted in order to evaluate the efficacy of standardized transmission with AnesList©.

Trial sites (1)

FacilityCityRegionStatus
Department of Anesthesia and Intensive Care - Ambroise Paré Hospital - APHP Boulogne-Billancourt France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05440331 on ClinicalTrials.gov ↗ ← All trials in France