Skip to main content
Clinical Trials/NCT02696135
NCT02696135
Recruiting
Not Applicable

The Chinese Hypertrophic Cardiomyopathy Study(CHCS)

China National Center for Cardiovascular Diseases1 site in 1 country3,000 target enrollmentMarch 23, 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiomyopathy, Hypertrophic
Sponsor
China National Center for Cardiovascular Diseases
Enrollment
3000
Locations
1
Primary Endpoint
Cardiovascular deaths
Status
Recruiting
Last Updated
8 years ago

Overview

Brief Summary

Hypertrophic cardiomyopathy (HCM) is one of the most common inherited cardiac diseases, with a prevalence of ∼0.2%. Sudden cardiac death (SCD), heart failure and stroke are the major poor outcomes of HCM. Although about half of the patients were found to be caused by mutations mainly located in genes encoding sarcomere proteins, the causes in a significant proportion of patients with HCM are still unknown. Even in the patients with sarcomere mutations, the molecular pathways that eventually lead to cardiac hypertrophy are remained to be revealed. Furthermore, HCM presents with significant heterogeneity. SCD risk stratification and prevention by ICD are necessary. However, the strategy of SCD risk stratification recommended by the 2011 ACCF/AHA and 2014 ESC guidelines were based mainly on the evidence derived from American and European countries. The accuracy of these guidelines in Chines patients with HCM was not evaluated yet.

Detailed Description

In the present study, patients with HCM are recruited prospectively after informed consent was given. The investigator will collect the baseline clinical characteristics of the patients at enrollment, including comprehensive physical examination, laboratory testing of blood and urine, electrocardiography, 24-hr Holter, echocardiography, MRI and other examinations if necessary. The specimens retained include blood for all patients and myocardium for patients receive surgery of myocardial myectomy. Multi-omics screening, including genomics, epigenomics, transcriptomics, proteomics, metabolomics, will be performed to identified novel disease genes, signal pathway or processes, genetic risk factors and potential therapy targets of HCM. Furthermore, besides examining the accuracy of SCD risk prediction of the 2011 ACCF/AHA and 2014 ESC guidelines, we will identify novel risk factors associated with the clinical outcomes and construct predictive models suitable for Chinese patients with HCM.

Registry
clinicaltrials.gov
Start Date
March 23, 2011
End Date
December 31, 2028
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
China National Center for Cardiovascular Diseases
Responsible Party
Principal Investigator
Principal Investigator

Lei.Song@NCCD

MD.&ph.D

China National Center for Cardiovascular Diseases

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Cardiovascular deaths

Time Frame: an average of 2 years

Including SCD and deaths due to heart failure and stroke.

Secondary Outcomes

  • all-cause mortality(an average of 2 years.)
  • Heart failure(an average of 2 years)
  • Stroke(an average of 2 years)
  • Malignant arrhythmia(an average of 2 years)

Study Sites (1)

Loading locations...

Similar Trials