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

Not Applicable

Completed

• Conditions: Hypotension During Surgery

• Registration Number: NCT06439732
• Lead Sponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCS

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

Study Timeline

• Study First Submitted: 2024-05-22
• Study First Submitted QC: 2024-05-27
• Study First Posted: 2024-06-03
• Study Start: 2024-07-01
• Primary Completion: 2025-05-01
• Status Verified: 2025-06
• Study Completion: 2025-06-01
• Last Update Submitted: 2025-07-08
• Last Update Posted: 2025-07-09

Recruitment & Eligibility

• Status: COMPLETED
• 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

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