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An Assessment of Pulse Pressure Variation to Guide Fluid Therapy in Cardiac Surgery Patients

A

Austin Health

Status and phase

Completed
Phase 2

Conditions

Cardiac Surgery

Treatments

Other: IV fluid according to PPV
Other: fluids according to standard care

Study type

Interventional

Funder types

Other

Identifiers

NCT01681758
AICU2012-007

Details and patient eligibility

About

We aim to test the hypothesis that fluid therapy based on pulse pressure variation (PPV) in patients after cardiac surgery who are mechanically ventilated leads to a significant decrease in the amount of fluid given to such patients in the first 24 hours after surgery

Full description

  1. The investigators will study patients after cardiac surgery
  2. The investigators will collect data on standard care in pre-intervention population
  3. The investigators will collect demographic and clinical data
  4. The investigators will collect biochemical data in the first 24 hours after surgery
  5. The investigators will collect biochemical, physiological and clinical outcome data
  6. The investigators will compare the standard care and intervention period data

Enrollment

104 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. immediately after ICU admission after cardiac surgery
  2. mandatory mechanical ventilation -

Exclusion criteria

  1. Pressure support ventilation
  2. ECMO
  3. Intra-aortic balloon counterpulsation

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

104 participants in 2 patient groups, including a placebo group

PPV
Active Comparator group
Description:
use PPV to guide fluid therapy
Treatment:
Other: IV fluid according to PPV
standard care
Placebo Comparator group
Description:
fluids according to standard care
Treatment:
Other: fluids according to standard care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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