Informations générales (source: ClinicalTrials.gov)
Morbidity and Mortality in Operating Room: Surgery and Standardized Communication (HIATUS)
Observational
Assistance Publique - Hôpitaux de Paris (Voir sur ClinicalTrials)
septembre 2023
décembre 2025
29 juin 2024
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.
Etablissements
| Les établissements d'Île-de-France ayant mis à jour leurs données Origine et niveau de fiabilité des données | |||||
|---|---|---|---|---|---|
| AP-HP - Hôpital Ambroise Paré | FLETCHER Dominique | 18/04/2025 07:55:45 | Contacter | ||
| AP-HP - Hôpital Bichat | FLETCHER Dominique | 18/04/2025 07:55:45 | Contacter | ||
| AP-HP - Hôpital La Pitié-Salpêtrière | FLETCHER Dominique | 18/04/2025 07:55:45 | Contacter | ||
| AP-HP - Hôpital Lariboisiere-Fernand Widal | FLETCHER Dominique | 18/04/2025 07:55:45 | Contacter | ||
| AP-HP - Hôpital Raymond Poincaré | FLETCHER Dominique | 18/04/2025 07:55:45 | Contacter | ||
| AP-HP - Hôpital Saint Antoine | FLETCHER Dominique | 18/04/2025 07:55:45 | Contacter | ||
| CLCC INSTITUT GUSTAVE ROUSSY | Migena DEMIRI | 06/03/2024 14:15:47 | Contacter | ||
| CLCC RENE HUGUENIN INSTITUT CURIE | 10/04/2025 13:12:05 | Contact (sur clinicalTrials) | |||
| Les établissements d'Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
| HOPITAL FOCH | jeudi 19 juin 2025 | Contact (sur clinicalTrials) | |||
| Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
| Department of Anesthesia and Intensive Care - Ambroise Paré Hospital - APHP - 92100 - Boulogne-Billancourt - France | Contact (sur clinicalTrials) | ||||
Critères
Tous
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.
- 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.
- 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.