← Eichor
Study identifier: NCT06014138 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Volatile Sedation for Patients With the Acute Respiratory Distress Syndrome

Condition: Acute Respiratory Distress Syndrome · Mechanical Ventilation Complication · Sedation Complication  ·  Sponsor: Guy's and St Thomas' NHS Foundation Trust

PhasePhase 2/Phase 3
Planned participants20
Who can joinAll sexes, 17 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Guy Glover  ·  00447879696250  ·  guy.glover@gstt.nhs.uk

Gill Radcliffe  ·  02071887188  ·  gillian.radcliffe@gstt.nhs.uk

Always discuss trial participation with your own doctor first.

Locations (1)

Guy's & St Thomas' NHS Foundation TrustLondon, London, United KingdomRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06014138