Improving prevention and treatment strategies for cardiomyopathy patients

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to create a natural population cohort of patients with various types of cardiomyopathy by enrolling participants from multiple centers. It will collect clinical data and biological samples from surgical patients to develop a prognostic system for cardiomyopathy. The study seeks to optimize risk stratification and explore new strategies for early prevention and treatment, ultimately enhancing the diagnosis and treatment efficiency for cardiomyopathy patients.

Why it matters

Who can join: the full rules

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.

Where it's running

• First Affiliated Hospital of Xi'an Jiantong University
  Xi'an, Shaanxi, China Recruiting

Study contacts

• Principal investigator: Yang Yan — First Affiliated Hospital Xi'an Jiaotong University
• Study coordinator: Yang Yan
• Email: yangyan3@xjtu.edu.cn
• Phone: +862985323869

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.