Ignite Creation Date:
2025-12-25 @ 5:04 AM
Ignite Modification Date:
2026-03-06 @ 4:45 AM
Study NCT ID:
NCT02852018
Status:
COMPLETED
Last Update Posted:
2018-01-23
First Post:
2016-07-21
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Identification of Genetic Markers Modulating Rhythmic Risk Among Patients With Severe Cardiomyopathy
Sponsor:
Nantes University Hospital
Organization:
Study Overview
Official Title:
Identification of Genetic Markers Modulating Rhythmic Risk Among Patients With Severe Cardiomyopathy
Status:
COMPLETED
Status Verified Date:
2018-01
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
GENECHOC
Brief Summary:
The aim of this project is to identify common genetic polymorphisms associated with the occurrence of rhythmic events in patients with severe cardiomyopathy.
Detailed Description:
None
Study Oversight
Has Oversight DMC:
False
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?: