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Volatile Sedation for Patients With the Acute Respiratory Distress Syndrome

Study acronym: ISO-DRIVE
StatusRecruiting
PhasePhase 2/3
Started
View on ClinicalTrials.gov ↗

Record History

  1. Primary completion date: Dec 31, 2024 to Jul 31, 2027
    • Study completion date: Mar 31, 2025 to Jul 31, 2027
    • Site details revised
    v3
  2. Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 1
    • Start date changed from estimate of Sep 30, 2023 to Nov 1, 2023
    v2
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This study will investigate how different types of routine sedation may affect patient's breathing whilst on a ventilator in the Intensive Care Unit (ICU). There are different approaches to sedation which may have advantages and disadvantages. During the study patients will receive both intravenous and inhaled volatile sedation (similar to anaesthetic 'gases' used for general anaesthesia) and the drive to breath, breathing efforts and function of the lung will be assessed.
Trial Details
NCT Number NCT06014138
Lead Sponsor Guy's and St Thomas' NHS Foundation Trust
Collaborators: Sedana Medical
Conditions
(from sponsor)		 Acute Respiratory Distress Syndrome, Mechanical Ventilation Complication, Sedation Complication
Related terms Respiratory Distress Syndrome
Enrollment 20 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov