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Clinical Trial Summary

The aim of the study is to answer a daily question in the operating room: what is the safest technique for intubation of severe/morbid obese patients (BMI 35 or more). There is a great heterogeneity of practices on the subject, so the principle is to determine a common practice to facilitate the management of these patients.


Clinical Trial Description

Anesthesia consultation or pre-anesthesia visit: - screening for inclusion and non-inclusion criteria - patient information - collection of consent - inclusion D0 (day of inclusion): - before general anesthesia : collection of epidemiological data (history + clinical examinations) + randomization (Arm A/Not Vent : intubation without ventilation or Arm B/Vent : intubation with ventilation) - general anesthesia : intubation according to randomization arm + collection primary endpoint + conduct of the intubation procedure + morbidity of the intubation procedure - after general anesthesia : collection of secondary endpoints + conduct of the intubation procedure + morbidity of the intubation procedure + intraoperative respiratory morbidity - post-interventional care room : collection of clinical parameters in the ICU : postoperative morbidity + study discharge (hospital discharge) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05930678
Study type Interventional
Source Nantes University Hospital
Contact Mickael VOURC'H, PhD
Phone 0244768053
Email mickael.vourch@chu-nantes.fr
Status Recruiting
Phase N/A
Start date September 12, 2023
Completion date September 12, 2025

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