Plain-English translation of NCT07145138 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Read our Heart Failure research guide →This is a research registry—a database—being built to understand dilated cardiomyopathy (a condition where the heart weakens and cannot pump blood effectively) across different racial and ethnic groups. Researchers want to find out whether certain genes that cause this disease are more common in some populations than others, and whether social, financial, and medical factors make the disease worse for some people. By collecting blood samples and health information from 1,500 participants, they hope to improve heart care for everyone, regardless of their background.
Most research on this type of heart disease has focused on white patients, leaving big gaps in understanding how the disease works and progresses in African American, Hispanic, Latino, and other minority populations. This study exists to fill that gap and ensure that treatments and care are fair and effective for all ethnic groups.
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You would visit a University of Illinois Chicago medical site where researchers would collect a blood sample from you and ask questions about your health history, family background, and living situation. You would share information from your medical records to help researchers understand how your condition has progressed. This is an observational study, meaning researchers are gathering information rather than testing a new treatment—you won't receive medication or special procedures as part of this study.
AI-generated summary from trial data · Jun 2, 2026 · Not medical advice
United States