Pediatric Cardiomyopathy Mutation Analysis

Part of paid clinical trials in Indianapolis, Indiana.

Sponsor
Indiana University
Study ID
NCT02432092
Status
Recruiting
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Conditions

Eligibility Criteria

Sex
ALL
Age
N/A - N/A
Healthy Volunteers
Not accepted

Study Details

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.

Key Dates

Start date
Apr 30, 2014
Status verified
Jun 2025
Primary completion
Dec 31, 2030
Completion
Dec 31, 2030

Study Design

Enrollment
300 participants (estimated)

Arms

  • Arm: Affected
    participants with cardiomyopathy
  • Arm: Family Members of affected
    Family members of participants with cardiomyopathy (can be affected or unaffected)

Primary Outcome Measure

Elucidate the molecular genetics of cardiomyopathy [ Time Frame: 7 years ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
IU School of MedicineIndianapolisIndiana46202
Stephanie Ware, MD, PhD
[email protected]
317-278-2807

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By research site
IU School of Medicine· Indianapolis, IN

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