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

> **NCT04014218** · PHASE4 · UNKNOWN · sponsor: **Moscow Regional Research and Clinical Institute (MONIKI)** · enrollment: 80 (estimated)

## Conditions studied

- ARDS

## Interventions

- **DRUG:** Inhalation Sedation
- **DRUG:** Intravenous Sedation

## Key facts

- **NCT ID:** NCT04014218
- **Lead sponsor:** Moscow Regional Research and Clinical Institute (MONIKI)
- **Sponsor class:** OTHER_GOV
- **Phase:** PHASE4
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2019-01-08
- **Primary completion:** 2019-09
- **Final completion:** 2020-01
- **Target enrollment:** 80 (ESTIMATED)
- **Last updated:** 2019-07-10

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04014218

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT04014218, "Effect of Inhalation Sedation Compared With Propofol on the Sepsis-related Acute Respiratory Distress Syndrome Course". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT04014218. Licensed CC0.

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