Arterial dP/dt Dependency on Loading Conditions

RESPONSE OF ARTERIAL dP/dt TO FLUIDS AND VASOACTIVE DRUGS DURING ABDOMINAL SURGERY: A PROSPECTIVE PILOT STUDY

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT06164405

Acronym

REABILITY

Enrollment

Registered

2023-12-11

Start date

2024-02-01

Completion date

2025-03-10

Last updated

2025-04-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intraoperative Hemodyamic Monitoring

Keywords

emodinamica

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

Interventions

DEVICEarterial dp/dtmax

to assess the variations of the arterial dp/dt max after drugs or fluids administration

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 85 Years

Healthy volunteers

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

Design outcomes

Primary

Measure	Time frame	Description
dp/dt fluids dependency	intraoperative	measurement of dp/dtmax after fluid challenge

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026