Status:
UNKNOWN
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives
Lead Sponsor:
D'Or Institute for Research and Education
Conditions:
Channelopathies
Eligibility:
All Genders
Brief Summary
several genes have been associated with ion channel diseases, but a large number of families do not yet have an identified genetic cause. There is a lack of information on the genetic characteristics ...
Detailed Description
Inherited arrhythmias are characterized by variable expressiveness and incomplete penetrance. Extensive genotype-phenotype studies are needed to elucidate the genetic basis of these diseases. There ar...
Eligibility Criteria
Inclusion
- Patients from Rede D'or São Luiz and their relatives
- Patients whit arrhythmia and their relatives
- Presence of inheritance pattern of causal genetic variants or those associated with phenotypes jointly defined as cardiac channelopathies and their relatives
Exclusion
- None
Key Trial Info
Start Date :
January 1 2018
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
July 31 2024
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT04832126
Start Date
January 1 2018
End Date
July 31 2024
Last Update
April 6 2021
Active Locations (1)
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1
D'Or Institute for Research and Education (IDOR)
Rio de Janeiro, Brazil, 22281-100