Project to improve cardiovascular health through biobanking
Official title: Cardiovascular Health Improvement Project
Run by University of Michigan · NCT02306200 · Data updated 2026-11-12
This project is collecting blood samples and health information from people with heart diseases and healthy individuals to help researchers learn more about heart health and its genetic factors.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 15000 (estimated) |
| Sponsor | University of Michigan Academic / other |
| Locations | 1 site (Ann Arbor, Michigan) |
| Status | Recruiting |
| Started | August 2013 |
| Main results expected | August 2053 |
| Study ends | August 2053 |
| Registry record updated | April 29, 2026 |
| Trial ID | NCT02306200 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adults over 18 with aortic pathology, cardiovascular disease, or healthy individuals without cardiovascular issues.
✕Probably not a fit
Patients who are unwilling or unable to provide informed consent will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This project aims to create a biobank that collects clinical information, DNA, plasma, and aortic tissue samples from patients with various cardiovascular diseases, as well as healthy controls. The study will gather biological specimens and family history to establish a comprehensive database that researchers can use for future studies. By providing well-annotated DNA samples along with demographic and clinical information, the project seeks to enhance understanding of cardiovascular conditions and their genetic underpinnings.
Why it matters
Potential benefit: If successful, this project could lead to improved understanding and treatment of cardiovascular diseases.
How similar studies have gone: Other studies have successfully established biobanks for cardiovascular research, indicating a promising approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Any patient over the age of 18 who is able/willing to give informed consent * Patients \<18 years of age with parental consent and assent (if assent is applicable for their age) * Diagnosis of: * aortic pathology potentially due to a known or suspected inherited condition * Idiopathic aortic aneurysm * Interesting of novel vascular pathology in the aorta or main branches * Family history of aortic or vascular disease * Other cardiovascular disease * Healthy controls with no apparent cardiovascular disease Exclusion Criteria: \- Not willing or able to sign the consent
Where it's running
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University of Michigan
Ann Arbor, Michigan, United States Recruiting
Study contacts
- Principal investigator: Marion A Hofmann Bowman, PhD, MD — University of Michigan
- Study coordinator: Lauren Humphrey-Stark, BS
- Email: ljeany@med.umich.edu
- Phone: 7342324779
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.