Identification of Genetic Markers Modulating Rhythmic Risk Among Patients With Severe Cardiomyopathy
NCT02852018 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1500
Last updated 2018-01-23
Summary
The aim of this project is to identify common genetic polymorphisms associated with the occurrence of rhythmic events in patients with severe cardiomyopathy.
Conditions
Interventions
- GENETIC
-
Identification of genetic polymorphisms
Sponsors & Collaborators
-
Nantes University Hospital
lead OTHER
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2010-01-31
- Primary Completion
- 2017-11-30
- Completion
- 2017-11-30
Countries
- France
Study Locations
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