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Clinical Trial Summary

Prospective, open-label, single-center, study to investigate the effect of sevoflurane sedation compared to a propofol-controlled arm during COPD exacerbation requiring invasive mechanical ventilation in ICU. Primary outcome measure: Evolution of airway resistance before and after sevoflurane in COPD patients, Secondary outcomes measures: Respiratory mechanics (Maximum pressure, PEEPi and PEEPtot, trapped volume), Gas exchange by the help of blood gases, The heterogeneity of alveolar ventilation by electro-impedancemetry, Evolution of pulmonary inflammation, Trophicity and contractility of the diaphragm,


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03460015
Study type Interventional
Source University Hospital, Montpellier
Contact
Status Terminated
Phase N/A
Start date March 1, 2018
Completion date December 16, 2020

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