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Fluid ORiented Therapy for yoUNg Asa 1patients

Not Applicable
Completed
Conditions
Hemodynamics
Interventions
Device: FloTrac
Registration Number
NCT03090399
Lead Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Brief Summary

In this retrospective analysis investigators will study the effects of using a minimally invasive hemodynamic monitoring (FloTrac-Edwards) on postoperative outcomes. Participants will compare a control group to a case group; in both groups ASA 1 patients suffering from advanced ovarian cancer underwent radical cytoreductive surgery. In case group hemodynamic was managed by using the FloTrac system; in the control group a standard hemodynamic monitoring was used.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
60
Inclusion Criteria
  • ASA 1
Exclusion Criteria
  • cardiac diseases
  • pulmonary diseases
  • renal diseases
  • metabolic disorders

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
case groupFloTracpatients in which fluids were administered according to FloTrac parameters
Primary Outcome Measures
NameTimeMethod
prevalence of complicationsup to 30 days
Secondary Outcome Measures
NameTimeMethod
days of hospitalizationup to 12 weeks
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