Arterial dP/dt Dependency on Loading Conditions

Completed

• Conditions: Intraoperative Hemodyamic Monitoring

• Registration Number: NCT06164405
• Lead Sponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Brief Summary

In the present study the investigators aim to assess the changes of the arterial dP/dtmax induced by fluids and vasoactive drugs during abdominal surgery

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2023-12-01
• Study First Submitted QC: 2023-12-01
• Study First Posted: 2023-12-11
• Study Start: 2024-02-01
• Primary Completion: 2025-02-01
• Study Completion: 2025-03-10
• Status Verified: 2025-04
• Last Update Submitted: 2025-04-04
• Last Update Posted: 2025-04-08

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 88

Inclusion Criteria

patients scheduled for abdominal surgery informed consent acceptance

Exclusion Criteria

• BMI> 30 Kg /m2;
• Atrial Fibrillation;
• Congestive heart failure with FE <35% and/or NYHA≥3;
• Severe known cardiac valve disease;
• Emergency surgery
• Shock or any acute conditions who required admission intensive care unit

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
dp/dt fluids dependency	intraoperative	measurement of dp/dtmax after fluid challenge

Trial Locations

Locations (1)

Fondazione Policlinico Universitairo Agostino Gemelli; 🇮🇹 Roma, RM, Italy