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Trial · NCT03395951

Registered outcomes18

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryChange in mean systemic filling pressure (mmHg)Baseline, every 5 minutes up to 30 minutes, 1 hour, 2 hoursDecrease or increase in mean systemic filling pressure measured by bedside continuous hemodynamic monitor supplied with continuous cardiac output monitoring with PiCCO(R) device
SecondaryChange in cardiac index (L/min/m2)Baseline, every 5 minutes up to 30 minutes, 1 hour, 2 hoursDecrease/increase in cardiac index measured by bedside continuous hemodynamic monitor supplied with continuous cardiac output monitoring with PiCCO(R) device
SecondaryChange in mean arterial pressure (mmHg)Baseline, every 5 minutes up to 30 minutes, 1 hour, 2 hoursDecrease/increase in mean arterial pressure measured by bedside continuous hemodynamic monitor supplied with continuous cardiac output monitoring with PiCCO(R) device
SecondaryChange in central venous pressure (mmHg)Baseline, every 5 minutes up to 30 minutes, 1 hour, 2 hoursDecrease/increase in central venous pressure measured by bedside continuous hemodynamic monitor supplied with continuous cardiac output monitoring with PiCCO(R) device
SecondaryChange in pressure for venous return (mmHg)Baseline, every 5 minutes up to 30 minutes, 1 hour, 2 hoursDecrease/increase in pressure for venous return measured by bedside continuous hemodynamic monitor supplied with continuous cardiac output monitoring with PiCCO(R) device
SecondaryChange in resistance to venous return (dynes⋅sec⋅cm-5)Baseline, every 5 minutes up to 30 minutes, 1 hour, 2 hoursDecrease/increase in resistance te venous return measured by bedside continuous hemodynamic monitor supplied with continuous cardiac output monitoring with PiCCO(R) device
SecondaryChange in systemic vascular resistance index (dynes⋅sec⋅cm-5)Baseline, every 5 minutes up to 30 minutes, 1 hour, 2 hoursDecrease/increase in systemic vascular resistance index measured by bedside continuous hemodynamic monitor supplied with continuous cardiac output monitoring with PiCCO(R) device
SecondaryChange in venous return index (L/min/m2)Baseline, every 5 minutes up to 30 minutes, 1 hour, 2 hoursDecrease/increase in venous return index measured by bedside continuous hemodynamic monitor supplied with continuous cardiac output monitoring with PiCCO(R) device
SecondaryChange in heart rate (bpm)Baseline, every 5 minutes up to 30 minutes, 1 hour, 2 hoursDecrease/increase in heart rate measured by bedside continuous hemodynamic monitor supplied with continuous cardiac output monitoring with PiCCO(R) device
SecondaryChange in extra vascular lung water index (mL/kg)Baseline and after 24 hoursDecrease/increase in extra vascular lung water index measured with continuous cardiac output monitoring PiCCO(R) device
SecondaryChange in global end diastolic volume index (mL/m2)Baseline and after 24 hoursDecrease/increase in global end diastolic volume index measured with continuous cardiac output monitoring PiCCO(R) device
SecondaryChange in intrathoracic blood volume index (mL/m2)Baseline and after 24 hoursDecrease/increase in intrathoracic blood volume index measured with continuous cardiac output monitoring PiCCO(R) device
SecondaryCreatinin (renal function) mmol/LBaseline and after 24 hoursIncrease/decrease in creatinin (standard blood withdrawal within standard ICU treatment)
SecondaryElectrolyte balance (potassium, sodium levels) (mmol/L)Baseline and after 24 hoursIncrease/decrease in electrolyte balance (potassium, sodium levels) (standard blood withdrawal within standard ICU treatment)
SecondaryDiuresis per hour (mL/hour)Baseline, 1 hour, 2 hours and after 24 hoursIncrease/decrease in diuresis (standardly measured within standard ICU treatment)
SecondaryBody weight (kg)Baseline and after 24 hoursIncrease/decrease in body weight (standardly measured within standard ICU treatment)
SecondaryFluid balance (mL)Baseline and after 24 hoursIncrease/decrease in fluid balance (mL) (standardly measured within standard ICU treatment)
SecondaryChange in cardiac performance (eH) (dimensionless)Baseline, every 5 minutes up to 30 minutes, 1 hour, 2 hoursIncrease/decrease in cardiac performance (eH)

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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