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Fluid ORiented Therapy for yoUNg Asa 1patients

I

Institute of Hospitalization and Scientific Care (IRCCS)

Status

Completed

Conditions

Hemodynamics

Treatments

Device: FloTrac

Study type

Interventional

Funder types

Other

Identifiers

NCT03090399
FORTUNA study

Details and patient eligibility

About

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.

Enrollment

60 patients

Sex

Female

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ASA 1

Exclusion criteria

  • cardiac diseases
  • pulmonary diseases
  • renal diseases
  • metabolic disorders

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

control group
No Intervention group
Description:
patients in which standard fluid administration was applied
case group
Active Comparator group
Description:
patients in which fluids were administered according to FloTrac parameters
Treatment:
Device: FloTrac

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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