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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06439732
Acronym
HERMES
Enrollment
84
Registered
2024-06-03
Start date
2024-07-01
Completion date
2025-06-01
Last updated
2025-08-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypotension During Surgery

Keywords

Anestethic comsumption, hemodynamic monitoring

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

Interventions

DEVICEAcumen IQ cuff

Use of Acumen IQ cuff for haemodynamic monitoring

Sponsors

Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* over 18 years of age * signature of informed medical consent

Exclusion criteria

* BMI\> 30 * eGFR\<30 * NYHA III-IV * severe cardiac valvular diseases * absence of informed medical consent

Design outcomes

Primary

MeasureTime frame
Reduction in Anesthetic consumptionDuring surgery

Secondary

MeasureTime frame
number hypotensive episodesduring surgery
duration hypotensive episodesduring surgery

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026