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Trial · NCT07896967

Registered outcomes16

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

ListOutcomeTime frameDescription
PrimarySuccessful liberation from mechanical ventilation within 28 days of enrollment28 daysDefined as the time from entry into the transition phase (study enrollment) to the first episode of sustained extubation, lasting at least 7 days
SecondaryVentilator free days (at day 28)28 daysNumber of ventilator free days at day 28
SecondaryICU length of stay (28 days)28 daysLength of ICU stay, measured in days from enrollment
SecondaryICU length of stay (at day 90)90 daysICU length of stay, measured in days from enrollment
SecondaryMortality at day 2828 daysMortality at day 28
SecondaryMortality at day 9090 daysMortality at day 90
SecondaryIncidence of weaning failure or reintubation7 daysreintubation within 7 days after extubation.
SecondaryRate of complications28 daysincluding tracheostomy and resumption of sedatives
SecondaryPhysiological characterization7 daysbased on different inspiratory effort levels (ΔPocc)
SecondaryIncidence (AI) of patient-ventilator asynchrony7 daysNumber of asynchronous respiratory cycles, expressed as a proportion of the total respiratory cycles recorded, overall and by PVA type.
SecondaryMechanical ventilation settings7 days
Main parameters obtained from the mechanical ventilator to describe the population such as Tidal volume (liters), PEEP(cmH2O), peak pressure (cmH2O), pressure support (cmH2O), inspiratory time (seconds), respiratory rate (n/min), FIO2 (%), plateau pressure(cmH2O), driving pressure(cmH2O), static compliance (ml/cmH20)
SecondaryGas exchange parameters7 dayse.g. PaO2 (mmhg), PaCO2 (mmhg) bicarbonate (mEq/L)
SecondaryRelevant medication7 dayse.g. vasoactive agents, delirium related medication
SecondaryIllness severity score (SOFA-score)7 daysSOFA-score. This score ranges from 0-24, with increasing scores reflecting more abnormal physiology and biochemistry or an increasing degree of intervention.
SecondaryUse of sedatives (cumulative dose and type)7 days
SecondaryReported delirium7 daysCAM-ICU

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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