Volume Responsiveness Assesment After Propofol.

CompletedOBSERVATIONAL
Enrollment

50

Participants

Timeline

Start Date

September 1, 2017

Primary Completion Date

September 1, 2020

Study Completion Date

September 1, 2020

Conditions
Circulatory FailureFluid Volume DisorderCritical Illness
Interventions
DRUG

Propofol bolus

Each patient gets propofol bolus in three doses. 0.25 mg/kg, 0.5 mg/kg and 1 mg/kg. After each dose patient's blood pressure, heart rate and haemodynamic values calibrated with PICCO device (cardiac output, cardiac index, stroke index, stroke volume, stroke volume variation, dPmax) are recorded in 15 seconds intervals for 10 minutes.

Trial Locations (1)

Unknown

Medical University of Gdańsk - Departament of Anesthesiology and Intensive Care, Gdansk

All Listed Sponsors
lead

Medical University of Gdansk

OTHER

NCT03917446 - Volume Responsiveness Assesment After Propofol. | Biotech Hunter | Biotech Hunter