UnknownPhase 4

Effect of Inhalation Sedation Compared With Propofol on the Sepsis-related Acute Respiratory Distress Syndrome Course

Russia80 participantsStarted 2019-01-08

Plain-language summary

Investigation of effect of inhalation sedation by administration of Sevoflurane compared with Propofol on the moderate acute respiratory distress syndrome course in mechanically ventilated patients with sepsis.

Who can participate

Age range18 Years – 65 Years

SexALL

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Inclusion Criteria: * sepsis * ARDS * P/F Ratio 100-250 * start of mechanical ventilation Exclusion Criteria: * pregnancy * concomitant oncological disease * prior psychological impairment

What they're measuring

mortality

Timeframe: 28 days after ICU admission

ICU Length of stay (LOS)

Timeframe: 45 days after ICU admission

Length of mechanical ventilation (LMV)

Timeframe: 45 days after ICU admission

Trial details

NCT IDNCT04014218

SponsorMoscow Regional Research and Clinical Institute (MONIKI)

Sponsor typeOTHER_GOV

Study typeINTERVENTIONAL

Primary completion2019-09

Contact for this trial

Valery V Likhvantsev,

+7 (903) 623-59-82 lik0704@gmail.com

View on ClinicalTrials.gov More ARDS trials