Risk Stratification and New Early Prevention and Treatment Strategies for Patients With Cardiomyopathy (STRENGTH Trial): a National Multi-center, Retrospective-prospective, Cohort Study
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Cardiomyopathies
- Sponsor
- First Affiliated Hospital Xi'an Jiaotong University
- Enrollment
- 500
- Locations
- 1
- Primary Endpoint
- Change in the incidence of mortality rate
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
This study will include patients with different types of cardiomyopathy from multiple centers were prospectively enrolled in a retrospective study to establish a natural population cohort of cardiomyopathy patients. By collecting clinical data and biological samples from surgical patients, we will construct a prognostic system for cardiomyopathy, optimize risk stratification, explore new strategies for the early prevention and treatment of cardiomyopathy, and improve the efficiency of clinical cardiomyopathy patients' diagnosis and treatment.
Detailed Description
This study will include patients with different types of cardiomyopathy from multiple centers were prospectively enrolled in a retrospective study to establish a natural population cohort of cardiomyopathy patients. By collecting clinical data and biological samples from surgical patients, we will construct a prognostic system for cardiomyopathy, optimize risk stratification, explore new strategies for the early prevention and treatment of cardiomyopathy, and improve the efficiency of clinical cardiomyopathy patients' diagnosis and treatment.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Age \>18 years old.
- •The diagnosis of cardiomyopathy was confirmed by cardiac ultrasound, electrocardiogram, magnetic resonance angiography, pathological examination and gene sequencing.
- •Patients or their families agreed to participate in the study and authorized informed consent.
Exclusion Criteria
- •Incomplete clinical data.
- •Do not agree to the inclusion or refuse to authorize the informed consent.
Outcomes
Primary Outcomes
Change in the incidence of mortality rate
Time Frame: At diagnosis, before discharge (about 7 days), 1, 3, 6, 9 month, 1, 2, 3, 5, 10 year.
The survival status will be obtained from the medical records and phone calls to patients or their family members