Informations générales (source: ClinicalTrials.gov)
Multicenter, Randomized, Open Study, Assessing Prophylactic Noninvasive Ventilation in Intensive Care Unit vs Postoperative Standard Care for Patients With High Risk of Postoperative Pulmonary Complication With Preoperative ARISCAT Score (ANTICIPUSC)
Interventional
N/A
Institut Cancerologie de l'Ouest (Voir sur ClinicalTrials)
octobre 2017
juin 2019
29 juin 2024
Postoperative pulmonary complications are one of the most common complications after
surgery.
Noninvasive ventilation has been proposed post-operatively to prevent postoperative
pulmonary complications.
Prophylactic noninvasive ventilation performed systematically in a non-specific
population is without interest.
The difficulty for the practitioner is to target patients at higher risk of developing a
postoperative pulmonary complications in order to guiding them to a post-operative
specialized care pathway.
The use of the ARISCAT score, validated on a large European prospective cohort, makes it
possible to evaluate, preoperatively, the risk of occurrence of postoperative pulmonary
complication in the patient.
The hypothesis of the present research is that early postoperative preventive treatment
with noninvasive ventilation, in patients at risk of postoperative pulmonary
complications according to the preoperative evaluation according to the ARISCAT score,
could have an interest in reducing these complications with a superior efficiency over
standard techniques.
Etablissements
| Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
|---|---|---|---|---|---|
| Chu D'Angers - 49000 - Angers - France | Cyril SARGENTINI, MD | Contact (sur clinicalTrials) | |||
| Institut de Cancerologie de L'Ouest - 49000 - Angers - France | DENIS DUPOIRON, MD | 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 | |||||
| Ch Du Mans - 72037 - Le Mans - France | Sigrid Caron, MD | Contact (sur clinicalTrials) | |||
Critères
Tous
Inclusion Criteria:
- Patient 18 years of age or older
- Patient scheduled for surgery or considered semi-urgent (=pre-anesthesia
consultation <48h before the surgical procedure) under General Anesthesia or under
Loco-Regional Anesthesia
- Patient with an ARISCAT score higher than or equal to 45 - Obtaining the signed
written consent of the patient
- Patient affiliated to a social security scheme
- Patient 18 years of age or older
- Patient scheduled for surgery or considered semi-urgent (=pre-anesthesia
consultation <48h before the surgical procedure) under General Anesthesia or under
Loco-Regional Anesthesia
- Patient with an ARISCAT score higher than or equal to 45 - Obtaining the signed
written consent of the patient
- Patient affiliated to a social security scheme
- Minor patients, pregnant or lactating women
- Obstetrical interventions
- Surgery under Local Anesthesia or Peripheral Nerve,
- Interventions taking place outside an interventional room
- Interventions for previous surgical complications
- Second surgery during study
- Organ transplantation
- Patients already intubated in preoperative
- Outpatient surgery
- Refusal of participation or inability to issue informed consent
- Person deprived of liberty or adult under guardianship
- Participation in another interventional study