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Clinical Trials/NCT06439732
NCT06439732
Completed
Not Applicable

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

Fondazione Policlinico Universitario Agostino Gemelli IRCCS1 site in 1 country84 target enrollmentJuly 1, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hypotension During Surgery
Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Enrollment
84
Locations
1
Primary Endpoint
Reduction in Anesthetic consumption
Status
Completed
Last Updated
8 months ago

Overview

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

Registry
clinicaltrials.gov
Start Date
July 1, 2024
End Date
June 1, 2025
Last Updated
8 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

RUSSO ANDREA

principal investigator

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

  • NYHA III-IV
  • severe cardiac valvular diseases
  • absence of informed medical consent

Outcomes

Primary Outcomes

Reduction in Anesthetic consumption

Time Frame: During surgery

Secondary Outcomes

  • number hypotensive episodes(during surgery)
  • duration hypotensive episodes(during surgery)

Study Sites (1)

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