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Trial · NCT06658522

Registered outcomes15

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

ListOutcomeTime frameDescription
PrimaryPower per beatFrom enrollment to end of study at 24 weeksmean pulmonary arery pressure (mPAP) x stroke volume (SV)
PrimaryRight ventricular pulmonary artery couplingFrom enrollment to end of study at 24 weeksEnd systolic elastance (Ees)/ Arterial elastance (Ea) as derived from pressure-volume loops using right heart catheterization
SecondaryRight ventricular end systolic volumeFrom enrollment to the end of study at 24 weeksRight ventricular end systolic volume as measured by cardiac magnetic resonance imaging
SecondaryRight ventricular end diastolic volumeFrom enrollment to the end of study at 24 weeksRight ventricular end diastolic volume as measured by cardiac magnetic resonance imaging
SecondaryRight ventricular ejection fractionFrom enrollment to the end of study at 24 weeksRight ventricular ejection fraction as measured by cardiac magnetic resonance imaging
SecondaryRight ventricular massFrom enrollment to the end of study at 24 weeksRight ventricular mass as measured by cardiac magnetic resonance imaging
SecondaryStroke volumeFrom enrollment to the end of study at 24 weeksStroke volume as measured by cardiac magnetic resonance imaging derived aortic flow
SecondaryLeft ventricular end diastolic volumeFrom enrollment to the end of study at 24 weeksLeft ventricular end diastolic volume as measured by cardiac magnetic resonance imaging
SecondaryLeft ventricular end systolic volumeFrom enrollment to the end of study at 24 weeksLeft ventricular end systolic volume as measured by cardiac magnetic resonance imaging
SecondaryLeft ventricular ejection fractionFrom enrollment to the end of study at 24 weeksLeft ventricular ejection fraction as measured by cardiac magnetic resonance imaging
SecondaryLeft ventricular massFrom enrollment to the end of study at 24 weeksLeft ventricular mass as measured by cardiac magnetic resonance imaging
SecondaryEnd-systolic elastance (Ees)From enrollment to the end of study at 24 weeksEnd systolic elastance measured using pressure-volume loops derived from right heart catheteriazation
SecondaryArterial elastance (Ea)From enrollment to the end of study at 24 weeksArterial elastance measured using pressure-volume loops derived from right heart catheteriazation
SecondaryEnd-diastolic elastance (Eed)From enrollment to the end of study at 24 weeksEnd-diastolic elastance measured using pressure-volume loops derived from right heart catheteriazation
SecondaryRight ventricular fibrosisFrom enrollment to the end of study at 24 weeksRigh ventricular fibrosis derived from extracellular volume measurements using Modified Look-Locker inversion recovery MRI sequence

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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