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Trial · NCT07103655

Registered outcomes12

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

ListOutcomeTime frameDescription
PrimaryPercentage change in pressure gradient during the Valsalva maneuverWeek 36The percentage reduction in the pressure gradient at the site of left ventricular obstruction during the Valsalva maneuver at week 36, compared to baseline, as measured by echocardiography.
SecondaryAnterior papillary muscle to the interventricular septum distanceWeek 36Percentage Increase in the distance from the anterior papillary muscle to the interventricular septum
SecondaryLeft atrial global longitudinal strainWeek 36
Left Atrial Global Longitudinal Strain (LA GLS) is an echocardiographic parameter derived from speckle-tracking imaging that measures the longitudinal deformation of the left atrial myocardium throughout the cardiac cycle.
SecondaryLeft ventricular global longitudinal strainWeek 36
Left Ventricular Global Longitudinal Strain (LVGLS) is a sensitive echocardiographic parameter derived from speckle-tracking imaging that quantifies the myocardial deformation in the longitudinal direction. It reflects the shortening of myocardial fibers along the long axis of the left ventricle during systole.
SecondaryPercentage change in resting pressure gradientWeek 36The percentage reduction in the pressure gradient at the site of left ventricular obstruction at rest measured by echocardiography at week 36 compared to baseline.
SecondaryAbsolute change in pressure gradient during the Valsalva maneuverWeek 36The absolute decrease in number of the pressure gradient at the site of left ventricular obstruction during the Valsalva maneuver measured by echocardiography at week 36 compared to baseline.
SecondaryThe proportion of patients with a pressure gradient <30 mmHg during the Valsalva maneuverWeek 36The proportion of patients with a pressure gradient \<30 mmHg at the site of obstruction during the Valsalva maneuver at week 36.
SecondaryBNPWeek 36Number decrease in BNP levels from baseline to week 36.
SecondaryTroponin TWeek 36Number decrease in Troponin T levels from baseline to week 36.
SecondaryNew-onset atrial fibrillationFrom baseline to week 36Rate of new-onset atrial fibrillation in each group during the study period
SecondaryLVEF<50%From baseline to week 36
The proportion of patients in each group with LVEF \<50% accompanied by signs and symptoms of heart failure worsening and/or an increase in BNP of ≥30% compared to the previous measurement during the study period.
SecondaryLVEF<40%From baseline to week 36Rate of LVEF \<40% in each group during the study period.

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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