Analyzing genetic mutations in pediatric cardiomyopathy

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to gather information from children diagnosed with various forms of cardiomyopathy and their families to better understand the genetic factors involved in this heart condition. By focusing on the molecular genetics of pediatric cardiomyopathy, the study seeks to improve diagnostic accuracy and inform future genetic counseling. The research highlights the need for precise genetic diagnosis, as outcomes in children with cardiomyopathy can vary significantly based on the underlying genetic cause. The findings may lead to enhanced management strategies and novel treatment options for affected individuals.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Subjects with cardiomyopathy
* Family members of subjects with cardiomyopathy

Exclusion Criteria:

* Subjects without cardiomyopathy
* Family members of subjects without cardiomyopathy

Where it's running

• IU School of Medicine
  Indianapolis, Indiana, United States Recruiting

Study contacts

• Principal investigator: Stephanie Ware, MD, PhD — IU School of Medicine
• Study coordinator: Sarah Murphy, MPH
• Email: bankssk@iu.edu
• Phone: (317) 278-3026

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Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.