Clin2
NCT06948344Possibly a fitRecruiting

Genetics study for inherited heart muscle disease

CardiomyopathyWhole Genome Sequencing

Part of Heart & circulation clinical trials.

This study is looking for people with inherited heart muscle disease that may be genetic. It uses advanced genetic testing to better understand the cause.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
560 people
Ages
19 years and older
Study type
Observational

Who can take part

  • You are 19 years or older
  • You have been diagnosed with cardiomyopathy (heart muscle disease)
  • Your cardiomyopathy is suspected to be genetic, not from other causes like high blood pressure or alcohol
  • If you had genetic testing before with no answers, you can still join
  • A close family member has the same type of cardiomyopathy

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

Similar studies

Other trials that look related to this one.

NCT00138931Recruiting
Study genetics of inherited heart and muscle conditions

This study looks at genetic causes of inherited heart (cardiovascular) and muscle/nerve (neuromuscular) conditions. You may be asked about your family history and possibly genetic samples to help connect symptoms to specific genetic changes.

Chicago, Illinois
NCT01143454Recruiting
Study unusual heart conditions and related genetic traits

This study looks at people with unusual or rare heart problems, or people with a family history of these issues. Doctors and researchers may collect and study your blood or tissue (and possibly store samples) to learn what causes the condition and how it may affect the heart.

Washington D.C., District of Columbia
NCT02432092Recruiting
Genetic testing for heart muscle disease in children and families

This study looks at genetic (DNA) changes that may cause cardiomyopathy, a disease where the heart muscle is weakened. It may help families understand possible causes and inform future care.

Indianapolis, Indiana
NCT05750147Recruiting
Study for cardiomyopathy linked to family or genes

This study looks at people with cardiomyopathy (or related heart muscle conditions) and those who may be at risk because of family history or genetic test results. It may help researchers better understand who is likely to develop the condition and how best to monitor or support them.

London
NCT05569356Not yet recruiting
Study of genetic heart muscle disease and its outlook

This study looks at people with a genetic heart muscle condition called cardiomyopathy, which can cause irregular heartbeats. By studying your condition, doctors hope to better understand how it develops, how to predict its course, and how to improve diagnosis and treatment.

Paris
NCT06926127Recruiting
Genomic study for rare and genetic diseases

This study aims to use advanced genetic testing to better understand rare and genetic diseases. It may help find a diagnosis or guide personalized care for you or your child.

Rome, Lazio

Hear when a new Whole Genome Sequencing trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.