Actively Recruiting
UIC Multi-Ethnic DCM Registry
Led by University of Illinois at Chicago · Updated on 2025-08-28
1500
Participants Needed
1
Research Sites
755 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Dilated cardiomyopathy (DCM), a condition where the heart loses its ability to pump blood throughout the body, is a common cause of death in the United States (US). It affects minorities more frequently and appears to causes greater harm than Whites. However, almost all research related to DCM has been performed in Whites, where up to half of cases run in the family. Several genes have been identified that cause the disease, but we are unsure if these same genes are also responsible for DCM in African Americans or Hispanic/Latino patients. The impact of various medical, social, and financial stressors on the severity of the disease in ethnic minorities also remains unclear. The investigators believe that certain genes are more common in different racial and ethnic groups and the greater medical, social, and financial burden faced by minorities in the US leads to more harm from DCM in these groups. The overall goal of the project is to test whether ethnic minority patients carrying genes that cause DCM experience more adverse effects in part because of various medical, social, and financial burdens. The investigators will first establish the UIC Multi-ethnic DCM Biorepository to look for how often certain genes are found across different race-ethnicity and then ask the question if these genes impact the severity of DCM. Finally, the investigators will study how a person's environment can alter the course of their disease. Through this, the investigators hope and strive to ensure equal and adequate heart care for individuals regardless of their race-ethnicity.
CONDITIONS
Official Title
UIC Multi-Ethnic DCM Registry
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Must be at least 18 years of age and be admitted to or seen at a UIH site.
- Subjects must be willing and able to give written, informed consent
You will not qualify if you...
- Adults who are unable to provide consent
- Women who are pregnant at the baseline visit
- Prisoners
- Individuals who are not yet adults (infants, children, teenagers).
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Illinois Hospital & Health Sciences
Chicago, Illinois, United States, 60612
Actively Recruiting
Research Team
D
David Tofovic, M.D.
CONTACT
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
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here