Identification of Genetic Markers Modulating Rhythmic Risk Among Patients With Severe Cardiomyopathy

NCT02852018 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1500

Last updated 2018-01-23

No results posted yet for this study

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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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02852018 on ClinicalTrials.gov