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A multimodal assessment of the effectiveness of mavacatel in patients with obstructive hypertrophic cardiomyopathy

A multimodal assessment of the effectiveness of mavacatel in patients with obstructive hypertrophic cardiomyopathy

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500095275
Enrollment
Unknown
Registered
2025-01-04
Start date
2024-11-01
Completion date
Unknown
Last updated
2025-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertrophic Cardiomyopathy

Interventions

Mavacamten Group:None
Non-Mavacamten Group:None

Sponsors

The First Affiliated Hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. According to the AHA/ACC/AMSSM / 2024 HRS/secondary/SCMR hypertrophic cardiomyopathy guide diagnosed with obstructive HCM. 2. Age: >=18 years old 3. Genetic testing related to hypertrophic cardiomyopathy has been completed, excluding other hypertrophic phenotype heart diseases (such as Fabre's disease, amyloid cardiomyopathy, etc.)

Exclusion criteria

Exclusion criteria: 1. Patients who were unable to complete the study follow-up plan and lacked follow-up data; 2. Patients lacking imaging data (including echocardiography, coronary CT, cardiac enhanced magnetic resonance imaging (MRI), and fibroblast activating protein inhibitor (FAPI) imaging); 3. A combination of acute or chronic medical or psychiatric conditions, including recent (within the past year) combination of active suicidal ideation or behavior or abnormalities in laboratory tests, that may increase the risk of adverse events for study participants or interfere with study findings, and are judged by the investigator to be unsuitable for inclusion in the study; 4. Women who are pregnant or breastfeeding; 5. Consider patients with other hypertrophic phenotype cardiomyopathy (such as hypertensive, amyloidosis, etc.)

Design outcomes

Primary

MeasureTime frame
Left ventricular ejection fraction;Left ventricular outflow tract pressure;Cardiac biomarker;Myocardial strain;

Secondary

MeasureTime frame
Kansas City cardiomyopathy questionnaire score;

Countries

China

Contacts

Public ContactYing Liu

The First Affiliated Hospital of Dalian Medical University

18098875801@163.com+86 180 9887 5801

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026