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Trial · NCT07529938

Registered outcomes11

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

ListOutcomeTime frameDescription
PrimaryChange in Resting Left Ventricular Outflow Tract (LVOT) Peak Gradient at Week 30Baseline to Week 30Change from baseline in resting left ventricular outflow tract (LVOT) peak gradient measured by Doppler echocardiography (unit: mmHg). Higher values indicate greater obstruction.
SecondaryChange in Valsalva-Induced Left Ventricular Outflow Tract (LVOT) Peak Gradient at Week 30Baseline to Week 30Change from baseline in LVOT peak gradient induced by the Valsalva maneuver measured by Doppler echocardiography (unit: mmHg). Higher values indicate greater obstruction.
SecondaryProportion of Participants with Improvement in New York Heart Association (NYHA) Functional Classification at Week 30Baseline to Week 30
Proportion of participants achieving at least one class improvement in New York Heart Association (NYHA) functional classification compared with baseline. NYHA class ranges from I to IV, where higher classes indicate worse functional status.
SecondaryChange in N-terminal pro-B-type Natriuretic Peptide (NT-proBNP) Levels at Week 30Baseline to Week 30Change from baseline in N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels (unit: pg/mL). Higher values indicate worse cardiac function.
SecondaryChange in High-Sensitivity Cardiac Troponin I (hs-cTnI) Levels at Week 30Baseline to Week 30Change from baseline in high-sensitivity cardiac troponin I (hs-cTnI) levels (unit: ng/L). Higher values indicate greater myocardial injury.
SecondaryChange in Left Ventricular Ejection Fraction (LVEF) at Week 30Baseline to Week 30Change from baseline in left ventricular ejection fraction (LVEF) measured by echocardiography (unit: %). Higher values indicate better cardiac systolic function.
SecondaryChange in Tricuspid Annular Plane Systolic Excursion (TAPSE) at Week 30Baseline to Week 30Change from baseline in tricuspid annular plane systolic excursion (TAPSE) measured by echocardiography (unit: mm). Higher values indicate better right ventricular function.
SecondaryIncidence of Adverse EventsUp to Week 30Number and proportion of participants experiencing any adverse events.
SecondaryIncidence of Serious Adverse EventsUp to Week 30Number and proportion of participants experiencing serious adverse events.
SecondaryIncidence of Treatment Discontinuation Due to Adverse EventsUp to Week 30Number and proportion of participants who discontinued treatment due to adverse events.
SecondaryIncidence of Left Ventricular Ejection Fraction Reduction Below 50%Up to Week 30Number and proportion of participants with LVEF \<50% during treatment.

Source ClinicalTrials.govtrials-2026-11-12-0.4.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone 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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GET https://conductscience.org/api/trials/v1/NCT07529938/registered