Informations générales (source: ClinicalTrials.gov)
Impact on Adverse Events (AE) Occurrence of Two Types of Experience Feedback on AE Analysed During Local Morbidity Mortality Reviews (MMR), (by Multi Professional Simulation Education Versus Simple Diffusion of MMR Decisions) (RMM Simulation)
Observational
Hospices Civils de Lyon (Voir sur ClinicalTrials)
mai 2017
octobre 2021
29 juin 2024
After implementing a French version of a trigger tool validated for computerized
detection of adverse events in patient's medical record, the study will be performed in
three parallel randomized arms of three identical departments (each steaming from 6 types
of medical, surgical or obstetrical departments with a total of 18 departments involved).
This three arms will be: no intervention, education of department's staff by multi
professional in situ simulation (adapted to the discovered adverse events), or simple but
large diffusion of results and decisions of Morbidity Mortality Reviews.
The interventions will be performed during a two-years period.
Etablissements
| Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
|---|---|---|---|---|---|
| Hospices Civils de Lyon - Direction DOQRU - 69002 - Lyon - France | Bernard BUI-XUAN, MD, PhD | Contact (sur clinicalTrials) | |||
Critères
Tous
Inclusion Criteria:
- patients aged > 18 years old
- patients hospitalized in the involved departments during the two-years
intervention's period
- patients aged > 18 years old
- patients hospitalized in the involved departments during the two-years
intervention's period
- patient aged < 18 years old
- no other exclusion criteria