# Respiratory Effect of the LISA Method with Sedation by Propofol Versus Absence of Sedation.

> **NCT04016246** · PHASE3 · ACTIVE_NOT_RECRUITING · sponsor: **University Hospital, Grenoble** · enrollment: 233 (actual)

## Conditions studied

- Respiratory Distress Syndrome in Premature Infant

## Interventions

- **DRUG:** Propofol-Lipuro
- **DRUG:** Placebos

## Key facts

- **NCT ID:** NCT04016246
- **Lead sponsor:** University Hospital, Grenoble
- **Sponsor class:** OTHER
- **Phase:** PHASE3
- **Study type:** INTERVENTIONAL
- **Status:** ACTIVE_NOT_RECRUITING
- **Start date:** 2019-10-07
- **Primary completion:** 2024-03-18
- **Final completion:** 2026-10
- **Target enrollment:** 233 (ACTUAL)
- **Last updated:** 2024-12-12


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04016246

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT04016246, "Respiratory Effect of the LISA Method with Sedation by Propofol Versus Absence of Sedation.". Retrieved via AI Analytics 2026-05-27 from https://api.ai-analytics.org/clinical/NCT04016246. Licensed CC0.

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