Impact of Using an Hemodynamic Monitoring System on Anesthetic Consumption During Abdominal Surgery
Not Applicable
Recruiting
- Conditions
- Hypotension During Surgery
- Interventions
- Device: Acumen IQ cuff
- Registration Number
- NCT06439732
- 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
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 84
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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Intervention Acumen IQ cuff In this group we will use a continuous non-invasive hemodynamic monitoring system (Acumen IQ cuff)
- Primary Outcome Measures
Name Time Method Reduction in Anesthetic consumption During surgery
- Secondary Outcome Measures
Name Time Method number hypotensive episodes during surgery duration hypotensive episodes during surgery
Trial Locations
- Locations (1)
Fondazione Policlinico Universitario "A. Gemelli" IRCCS
🇮🇹Roma, Italy