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Trial · NCT07894393

Registered outcomes17

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

ListOutcomeTime frameDescription
PrimaryCardiac index10 minutes after endotracheal intubationCardiac index (L/min/m2) measured with the pressure recording analytical method (PRAM; MostCare Up) via a radial arterial line, compared between the four wash-in groups.
SecondarySystolic arterial pressureBefore induction (T0), 30 seconds after intubation (T1), when 0.8 MAC is reached (T2) and 10 minutes after intubation (T3)
Systolic arterial pressure (mmHg) measured with the pressure recording analytical method (PRAM; MostCare Up) via a radial arterial line. At each time point, the highest value among five consecutive beats was recorded.
SecondaryDiastolic arterial pressureBefore induction (T0), 30 seconds after intubation (T1), when 0.8 MAC is reached (T2) and 10 minutes after intubation (T3)
Diastolic arterial pressure (mmHg) measured with the pressure recording analytical method (PRAM; MostCare Up) via a radial arterial line. At each time point, the highest value among five consecutive beats was recorded.
SecondaryMean arterial pressureBefore induction (T0), 30 seconds after intubation (T1), when 0.8 MAC is reached (T2) and 10 minutes after intubation (T3)
Mean arterial pressure (mmHg) measured with the pressure recording analytical method (PRAM; MostCare Up) via a radial arterial line. At each time point, the highest value among five consecutive beats was recorded.
SecondaryHeart rateBefore induction (T0), 30 seconds after intubation (T1), when 0.8 MAC is reached (T2) and 10 minutes after intubation (T3)
Heart rate (beats/min) measured with the pressure recording analytical method (PRAM; MostCare Up) via a radial arterial line. At each time point, the highest value among five consecutive beats was recorded.
SecondaryCardiac index at other time pointsBefore induction (T0), 30 seconds after intubation (T1) and when 0.8 MAC is reached (T2)
Cardiac index (L/min/m2) measured with the pressure recording analytical method (PRAM; MostCare Up) via a radial arterial line. At each time point, the highest value among five consecutive beats was recorded.
SecondaryStroke volume indexBefore induction (T0), 30 seconds after intubation (T1), when 0.8 MAC is reached (T2) and 10 minutes after intubation (T3)
Stroke volume index (mL/m2) measured with the pressure recording analytical method (PRAM; MostCare Up) via a radial arterial line. At each time point, the highest value among five consecutive beats was recorded.
SecondaryPulse pressure variation30 seconds after intubation (T1), when 0.8 MAC is reached (T2) and 10 minutes after intubation (T3)
Pulse pressure variation (%) measured with the pressure recording analytical method (PRAM; MostCare Up) via a radial arterial line. At each time point, the highest value among five consecutive beats was recorded. Not assessed at T0 because patients were breathing spontaneously.
SecondaryCardiac cycle efficiencyBefore induction (T0), 30 seconds after intubation (T1), when 0.8 MAC is reached (T2) and 10 minutes after intubation (T3)
Cardiac cycle efficiency (unitless index, range -1 to +1) measured with the pressure recording analytical method (PRAM; MostCare Up) via a radial arterial line. At each time point, the highest value among five consecutive beats was recorded.
SecondaryMaximum rate of arterial pressure rise (dP/dt)Before induction (T0), 30 seconds after intubation (T1), when 0.8 MAC is reached (T2) and 10 minutes after intubation (T3)
Maximum rate of rise of the radial arterial pressure, dP/dt (mmHg/ms) measured with the pressure recording analytical method (PRAM; MostCare Up) via a radial arterial line. At each time point, the highest value among five consecutive beats was recorded.
SecondaryArterial elastanceBefore induction (T0), 30 seconds after intubation (T1), when 0.8 MAC is reached (T2) and 10 minutes after intubation (T3)
Arterial elastance (mmHg/mL) measured with the pressure recording analytical method (PRAM; MostCare Up) via a radial arterial line. At each time point, the highest value among five consecutive beats was recorded.
SecondaryCardiac power indexBefore induction (T0), 30 seconds after intubation (T1), when 0.8 MAC is reached (T2) and 10 minutes after intubation (T3)
Cardiac power index (W/m2) measured with the pressure recording analytical method (PRAM; MostCare Up) via a radial arterial line. At each time point, the highest value among five consecutive beats was recorded.
SecondaryWash-in durationFrom start of sevoflurane delivery until 0.8 MAC is reached (up to 10 minutes after intubation)Time (seconds) from the start of sevoflurane delivery after intubation until the age-adjusted MAC displayed by the anaesthesia workstation reaches 0.8.
SecondaryCumulative sevoflurane consumptionWhen 0.8 MAC is reached and 10 minutes after intubationCumulative liquid sevoflurane consumption (mL) as reported numerically by the anaesthesia workstation.
SecondaryNumber of participants requiring ephedrineFrom induction of anaesthesia to 10 minutes after intubationNumber of participants who received at least one 10-mg intravenous bolus of ephedrine for hypotension, defined as mean arterial pressure \<65 mmHg or a decrease \>30% from baseline.
SecondaryTime to first ephedrine administrationFrom induction of anaesthesia to 10 minutes after intubationTime (seconds) from induction of anaesthesia to the first intravenous ephedrine bolus given for hypotension (mean arterial pressure \<65 mmHg or a decrease \>30% from baseline).
SecondaryState entropy30 seconds after intubation (T1), when 0.8 MAC is reached (T2) and 10 minutes after intubation (T3)State entropy (units on a scale, 0-91) measured with the GE Entropy module; lower values indicate deeper hypnosis.

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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