Trials / Unknown
UnknownNCT03754101
Exome Sequencing Study in Cardiomyopathy to Identify New Risk Variants
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 4,000 (estimated)
- Sponsor
- Tongji Hospital · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Accepted
Summary
Genetic mutations has been proved to be associated wth the onset of cardiomyopathy. In the present study, we intend to identify new related variants or genes. From March, 2003 to November, 2017, patients diagnosed as cardiomyopathy were consecutively recruited, and their sampled were drawn from peripheral blood. Paired control group were also enrolled. The whole exome sequencing was used to find out the variants associated with the onset of cardiomyopathy and its prognosis.
Conditions
Timeline
- Start date
- 2003-03-03
- Primary completion
- 2025-10-31
- Completion
- 2025-10-31
- First posted
- 2018-11-27
- Last updated
- 2023-02-17
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT03754101. Inclusion in this directory is not an endorsement.