Plain-English translation of NCT00138931 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Researchers at the University of Chicago are trying to understand the genetic causes of inherited heart and muscle diseases like cardiomyopathy, arrhythmias, and muscular dystrophy. By studying DNA samples from patients and their families, they hope to identify which genetic mutations cause these conditions. This knowledge could eventually help doctors diagnose and treat these diseases more effectively.
Many people inherit heart and muscle diseases from their families, but scientists don't yet understand all the genetic changes that cause them. By collecting and analyzing genetic samples from affected families, researchers can discover which genes are responsible and potentially develop better treatments in the future.
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If you qualify, you would likely provide a blood sample (or possibly a tissue sample) that researchers can use to study your genetic material. You may also be asked to share your medical history and family history of disease. The study is recruiting up to 2,000 participants and their families, and your involvement would help scientists understand these inherited conditions better.
AI-generated summary from trial data · Jun 5, 2026 · Not medical advice
United States
Enrollment target
~2,000 participants
Started
September 1996
Primary completion
January 2030
Last updated on clinicaltrials.gov in September 2025.
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Central contact
Lisa Dellefave, MS
University of Chicago
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