Actively Recruiting

All Genders
ID02432092

Pediatric Cardiomyopathy Mutation Analysis

Led by Indiana University · Updated on 2025-06-26

300

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

I

Indiana University

Lead Sponsor

A

American Heart Association

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to identify the genetic causes of pediatric cardiomyopathy, a group of heart muscle disorders that affect how the heart pumps blood. Understanding the molecular genetics behind these conditions will help improve genetic counseling for affected families and contribute to understanding normal and abnormal heart function. The study focuses on children since the genetic diagnosis in this group is more complex compared to adults. Participants include children diagnosed with various types of cardiomyopathy as well as their family members, whether they have the condition or not. There are no interventions or treatments being tested, as this is an observational study aimed at collecting genetic information. The study does not involve any experimental therapies or procedures but gathers data to support future diagnosis and treatment strategies. Participants will provide genetic information that researchers will analyze over a period of seven years to better understand the genetics of cardiomyopathy. The study involves data collection from affected children and their relatives, which will help researchers learn about molecular causes of the disease. The results may guide future care and development of new treatments, but participants will not receive direct treatment through this study.

CONDITIONS

Brief Title

Pediatric Cardiomyopathy Mutation Analysis

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Subjects with cardiomyopathy
  • Family members of subjects with cardiomyopathy
Not Eligible

You will not qualify if you...

  • Subjects without cardiomyopathy
  • Family members of subjects without cardiomyopathy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Initial evaluation period

Participants undergo genetic testing to identify the molecular genetics of pediatric cardiomyopathy.

1 to 2 visits depending on genetic testing requirements

Long-term Monitoring

Duration - Up to 7 years

Participants are followed for ongoing observation to understand the genetic causes and outcomes of pediatric cardiomyopathy.

Periodic visits over several years for monitoring

Trial Site Locations

Total: 1 location

1

IU School of Medicine

Indianapolis, Indiana, United States, 46202

Actively Recruiting

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Research Team

L

Lindsey Helvaty, BS, BA

S

Stephanie Ware, MD, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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