Second Affiliated Hospital, Zhejiang University School of Medicine
Hangzhou, Zhejiang, 310009, China
NCT Number: NCT07103655
This study is a prospective interventional cohort study aimed at evaluating the therapeutic efficacy and clinical utility of Mavacamten-a targeted myosin inhibitor specifically developed for obstructive hypertrophic cardiomyopathy (HCM)-in patients with HCM characterized by mid-to-apical left ventricular obstruction.
Trial opening soon.
Get Notified18 year–75 year
All sexes
Interventional
Phase 4
Hangzhou, Zhejiang, 310009, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
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③Ability to provide written informed consent (ICF) and any required privacy authorization prior to study enrollment.
Exclusion criteria
-
Add Mavacamten to guideline-directed standard medical therapy for patients with hypertrophic cardiomyopathy (HCM) and mid-to-apical left ventricular obstruction.
Other names: beta receptor blockers
Administer an appropriate dose of beta-blockers according to the patient's tolerance.
Administer an appropriate dose of diltiazem according to the patient's tolerance.
Time frame: Week 36
The 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.
Time frame: Week 36
Percentage Increase in the distance from the anterior papillary muscle to the interventricular septum
Time frame: Week 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.
Time frame: Week 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.
Time frame: Week 36
The percentage reduction in the pressure gradient at the site of left ventricular obstruction at rest measured by echocardiography at week 36 compared to baseline.
Time frame: Week 36
The 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.
Time frame: Week 36
The proportion of patients with a pressure gradient <30 mmHg at the site of obstruction during the Valsalva maneuver at week 36.
Time frame: Week 36
Number decrease in BNP levels from baseline to week 36.
Time frame: Week 36
Number decrease in Troponin T levels from baseline to week 36.
Time frame: From baseline to week 36
Rate of new-onset atrial fibrillation in each group during the study period
Time frame: 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.
Time frame: From baseline to week 36
Rate of LVEF <40% in each group during the study period.
Contact information is provided by the study sponsor or research team.
Second Affiliated Hospital, School of Medicine, Zhejiang University
Other
The Therapeutic Value of Mavacamten in Hypertrophic Cardiomyopathy With Mid-to-Apical Left Ventricular Obstruction: A Prospective, Interventional, Real-World Clinical Study.
Acronym: BRAVE-HCM
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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