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Arterial dP/dt Dependency on Loading Conditions (REABILITY)

I

Institute of Hospitalization and Scientific Care (IRCCS)

Status

Completed

Conditions

Intraoperative Hemodyamic Monitoring

Treatments

Device: arterial dp/dtmax

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

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

Enrollment

88 patients

Sex

All

Ages

18 to 85 years old

Volunteers

No 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

Trial contacts and locations

1

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Central trial contact

andrea russo

Data sourced from clinicaltrials.gov

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