Clinical Trials Directory

Trials / Completed

CompletedNCT06439732

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
84 (actual)
Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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

Conditions

Interventions

TypeNameDescription
DEVICEAcumen IQ cuffUse of Acumen IQ cuff for haemodynamic monitoring

Timeline

Start date
2024-07-01
Primary completion
2025-05-01
Completion
2025-06-01
First posted
2024-06-03
Last updated
2025-08-22

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT06439732. Inclusion in this directory is not an endorsement.

Impact of Using an Hemodynamic Monitoring System on Anesthetic Consumption During Abdominal Surgery (NCT06439732) · Clinical Trials Directory