Impact of Using an Hemodynamic Monitoring System on Anesthetic Consumption During Abdominal Surgery
NCT ID: NCT06439732
Last Updated: 2025-08-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
84 participants
INTERVENTIONAL
2024-07-01
2025-06-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Intervention
In this group we will use a continuous non-invasive hemodynamic monitoring system (Acumen IQ cuff)
Acumen IQ cuff
Use of Acumen IQ cuff for haemodynamic monitoring
Control
In this group we will use the oscillometric non-invasive blood pressure monitoring system
No interventions assigned to this group
Interventions
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Acumen IQ cuff
Use of Acumen IQ cuff for haemodynamic monitoring
Eligibility Criteria
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Inclusion Criteria
* signature of informed medical consent
Exclusion Criteria
* eGFR\<30
* NYHA III-IV
* severe cardiac valvular diseases
* absence of informed medical consent
18 Years
ALL
No
Sponsors
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Fondazione Policlinico Universitario Agostino Gemelli IRCCS
OTHER
Responsible Party
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RUSSO ANDREA
principal investigator
Principal Investigators
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Andrea Russo, MD
Role: PRINCIPAL_INVESTIGATOR
Fondazione Policlinico universitario Agostino Gemelli
Locations
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Fondazione Policlinico Universitario "A. Gemelli" IRCCS
Roma, Roma, Italy
Countries
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Other Identifiers
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6704
Identifier Type: -
Identifier Source: org_study_id
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