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Clinical Trial Summary

The main objective will be to compare the number of ventilator-free days within the 28 days following the first spontaneous breathing trial between strategies of extubation performing spontaneous breathing trials with T-piece trials or with Pressure-Support trials. To do that, the study director proposed to conduct a prospective multicenter randomized controlled open-label trial comparing these 2 strategies of weaning in patients at high-risk of extubation failure in the Intensive Care Unit. Patients included will be randomized before performing the first spontaneous breathing trial and will be assigned to one of the following two groups according to the weaning strategy: T-piece trial group or Pressure-Support trial group.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04227639
Study type Interventional
Source Poitiers University Hospital
Contact
Status Completed
Phase N/A
Start date January 31, 2020
Completion date September 7, 2021

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