Taking people in United StatesNo phase
Studying Genetic Causes of Heart Muscle Disease in Children
Collects genetic information from children with heart muscle disease and their families.
Plain-language title generated from the registry record
Registry title: Pediatric Cardiomyopathy Mutation Analysis
Key facts
- Where
- Indianapolis, United StatesSee the site
Where in United States
- IU School of MedicineIndianapolis, United StatesTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Indiana University
- Trial code
- NCT02432092
- Record updated
- 22 June 2026
- Original description
The goal of this protocol is to obtain information from individuals with cardiomyopathy and from their families in order to elucidate the molecular genetics of this disorder. This will provide the basis for future genetic counseling as well as contribute to elucidating the biology of normal and abnormal cardiac function.Read full original descriptionShow less
Pediatric Cardiomyopathy Mutation Analysis
The goal of this protocol is to obtain information from individuals with cardiomyopathy and from their families in order to elucidate the molecular genetics of this disorder. This will provide the basis for future genetic counseling as well as contribute to elucidating the biology of normal and abnormal cardiac function.
Inclusion: Subjects with cardiomyopathy; Family members of subjects with cardiomyopathy.
Exclusion: Subjects without cardiomyopathy; Family members of subjects without cardiomyopathy.