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Trial · NCT06273397

Registered outcomes12

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

ListOutcomeTime frameDescription
PrimaryTreatment success4 daysComplete decongestion by the third morning without requiring escalation in diuretic therapy (by the second morning).
SecondaryMortality3 monthsAll-cause mortality during the first 3 months after start of the study
SecondaryWorsening Heart Failure3 monthsReadmission for Heart Failure or Urgent visit for Heart Failure during the first 3 months after start of the study
SecondaryCumulative 24-hour NatriuresisDay 2Natriuresis measured on the second day
SecondaryCumulative weight loss4 daysCumulative weight loss by the third morning
SecondarySubclinical congestion4 days
Congestion score will be the score used in the study to evaluate the primary outcome. The calculated scores can range from 0 to 12 points, with 0 indicating absence of congestion and 12 representing the highest degree of congestion. The primary outcome will be defined as achieving a score of 0 or 1 and also having absence of B-lines in the lung ultrasound (negative LUS criterion). In this secondary outcome, the presence of subclinical congestion will be evaluated, which is defined as a congestion score of 0 or 1 but with a positive LUS.
SecondaryChange in Hematocrit value4 daysChange in Hematocrit
SecondaryChange in NT-proBNP concentration4 daysChange in NT-proBNP
SecondaryChange in CA125 value4 daysChange in CA125
OtherAny adverse event3 monthsAny adverse clinical event related to intervention during the first 3 months after start of the study
OtherChanges in pH value4 daysChange in pH over the specified time period
OtherChange in plasma electrolyte values4 daysChange in plasma concentration of sodium, potassium, and chloride

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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