Outcome of Different Pathogenic Mutations in Hypertrophic Cardiomyopathy

Status Recruiting

Clinical Trial Summary

This is a prospective, single-center study to assess clinical phenotype and prognosis of different pathogenic mutations in Chinese patients with hypertrophic cardiomyopathy. Patients with hypertrophic cardiomyopathy were consecutively recruited, and then DNA samples were extracted from peripheral blood. Targeted sequencing of 142 genes was performed to obtain variants associated with hypertrophic cardiomyopathy. Patients will undergo face-to-face interviews, phone calls, or/and chart reviews at 6 months, 12 months, 24 months, 36 months, 48 months and 60 months for data collection of clinical outcomes.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03726424
Study type	Observational
Source	Tongji Hospital
Contact	Jia Qi Dai, MD candidate
Phone	86-27-83663280
Email	d201781397@hust.edu.cn
Status	Recruiting
Phase
Start date	February 25, 2011
Completion date	December 31, 2019

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