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

I

Institute of Hospitalization and Scientific Care (IRCCS)

Status

Not yet enrolling

Conditions

Hypotension During Surgery

Treatments

Device: Acumen IQ cuff

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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

Enrollment

84 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

84 participants in 2 patient groups

Intervention
Experimental group
Description:
In this group we will use a continuous non-invasive hemodynamic monitoring system (Acumen IQ cuff)
Treatment:
Device: Acumen IQ cuff
Control
No Intervention group
Description:
In this group we will use the oscillometric non-invasive blood pressure monitoring system

Trial contacts and locations

0

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Central trial contact

Andrea Russo, MD; Andrea Russo, MD

Data sourced from clinicaltrials.gov

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