← Eichor
Study identifier: NCT06639737 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Preoperative Blood Volume Optimization Using Transthoracic Echocardiography

Condition: Anesthesia · Anesthesia Complication · Anesthesia Induction  ·  Sponsor: University Hospital, Caen

PhaseNA
Planned participants220
Who can joinAll sexes, 18 Years to 99 Years
Healthy volunteersNo

About this study

Immediately following the induction of general anesthesia, arterial hypotension may occur with an incidence of about 40% in patients classified as ASA 3 or 4. Perioperative arterial hypotension is associated with increased perioperative morbidity and mortality. The increased mortality associated with perioperative arterial hypotension has been reported up to 30 and 90 days after surgery. This association appears to be both dose-dependent and time-dependent (severity and duration of arterial hypotension). EchOptimal study aims to determine whether non invasive preoperative stroke volume optimization using transthoracic echocardiography (TTE) can reduce the incidence and severity arterial hypotension following induction of general anesthesia. This is prospective, randomized, controlled, double blinded study approved by ethics comittee. The primary objective of this study is to compare the incidence of arterial hypotension (mean arterial pressure \< 65 mmHg) within the first 15 minutes following the induction of general anesthesia, between 2 groups : * standard current care (stroke volume optimized after induction of general anesthesia using oesophageal doppler) and * preopertaive stroke volume optimization using transthoracic echocardiography measument of subaortic velocity time integral.

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

Talk to the study team

jean-luc HANOUZ, MD PhD  ·  02 31 06 47 36  ·  hanouz-jl@chu-caen.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Universty Hospital of CaenCaen, Normandy, FranceRecruiting

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/NCT06639737