CardiomyopathiesGeneticsChildren's health
What this study is
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.
Study details
- Sponsor
- Indiana University
- Conditions
- Cardiomyopathies · Dilated Cardiomyopathy · Hypertrophic Cardiomyopathy · Restrictive Cardiomyopathy · Arrhythmogenic Right Ventricular Cardiomyopathy · Left Ventricular Non-compaction Cardiomyopathy
- Enrolling
- 300 people
- Starts
- 2014-04
- Est. completion
- 2030-12-31
- Record
- View on ClinicalTrials.gov ↗
Who can join
Sex ALLHealthy volunteers Not acceptedYou may qualify if
- Subjects with cardiomyopathy
- Family members of subjects with cardiomyopathy
You can't join if
- Subjects without cardiomyopathy
- Family members of subjects without cardiomyopathy
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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1
Study locations (1)
1 openIU School of Medicine
Indianapolis, Indiana, United States
- Stephanie Ware, MD, PhD · Contact317-278-2807stware@iu.edu
Recruiting
Study team
Sponsor
Indiana University
Study ID 1403919054
Principal investigator
Stephanie Ware, MD, PhD
IU School of Medicine
Have questions? The contacts above can answer them before you apply.
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.