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Clinical Trial 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.


Clinical Trial Description

The secondary objectives are: - to analysis the impact of the transmission on: 1. the occurence of different events: re-hospitalization, serious complications, death at one month; 2. the duration of initial ICU stay and of hospitalization; 3. the duration of the transmission; 4. the quality of the transmission by the physician leaving operating room. - to evaluate the condition of the transmission - to study the persistence of the use of the AnesList© at 6 months after the end of inclusions in the center - to evaluate the satisfaction on AnesList© and on the training with the tool and the obstacles of its utilization - to evaluate the morbility-mortality in the centers of the centers before, during and 6 months after the beginning of the study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05440331
Study type Observational
Source Assistance Publique - Hôpitaux de Paris
Contact Dominique FLETCHER, MD, PhD
Phone +33 (0)661177035
Email dominique.fletcher@aphp.fr
Status Recruiting
Phase
Start date September 8, 2023
Completion date December 2025

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