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Impact of Using an Hemodynamic Monitoring System on Anesthetic Consumption During Abdominal Surgery — HERMES  

Hypotension During Surgery Clinical Trial

Official title:
Impact of Using an Hemodynamic Monitoring System on Anesthetic Consumption During Abdominal Surgery

Clinical Trial Summary

In this study investigators will study the association between the use of an hemodynamic monitoring system and the anesthetic consumption in patients following major abdominal surgery. Investigators will randomise patients for a control group and an intervention group. Patients belonging to intervention group will be monitored with a non-invasively continue system (Acumen IQ cuff sensor), while the control group will be monitored with a non-invasive intermittent pressure system. The total amount of mL of Sevoflurane will be registered in both groups and the difference will be considered as the aim of our study

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06439732
Study type Interventional
Source Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Contact Andrea Russo, MD
Phone 0630154507
Email russoandreamd@gmail.com
Status Not yet recruiting
Phase N/A
Start date July 1, 2024
Completion date July 1, 2026
View Details
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