Viewing Study NCT06439732



Ignite Creation Date: 2024-06-16 @ 11:49 AM
Last Modification Date: 2024-10-26 @ 3:31 PM
Study NCT ID: NCT06439732
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-06-03
First Post: 2024-05-22

Brief Title: Impact of Using an Hemodynamic Monitoring System on Anesthetic Consumption During Abdominal Surgery
Sponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Organization: Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Study Overview

Official Title: Impact of Using an Hemodynamic Monitoring System on Anesthetic Consumption During Abdominal Surgery
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: HERMES
Brief 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
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: None