About this trial
We will enroll patients scheduled for abdominal aortic aneurysm repair and divide in two groups; in the control group the hemodynamic optimization will be made based on standard cardiovascular parameters showed in the Hemosphere platform. In the interventional group the hemodynamic optimization will be made based on the hypotension prediction index.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
planned aortic surgery acceptance of written informed consent
Disqualifiers
body mass index > 35 kg/m2
atrial fibrillation
urgent surgery
end-stage renal disease
Trial design
Parallel
Treatments tested in this trial
proactive therapy
Other interventiondrugs and fluids will be given based on the hypotension prediction index
Treatment groups
Trial outcomes
Primary outcomes
time weighted average of mean arterial presure under 65 mmHg
we will assess the magnitude of intraoperative arterial hypotension
Sponsors and contacts
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