Actively Recruiting
Vascular Disease Discovery Protocol
Led by National Heart, Lung, and Blood Institute (NHLBI) · Updated on 2026-05-01
1000
Participants Needed
1
Research Sites
980 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Background: Some genetic diseases put increase the risk of heart and blood diseases, which are the number one cause of death and disability in the U.S. Researchers want to study diseases of the heart and/or blood vessels. They want to collect data and specimens from affected people, their family members, and healthy people. Objective: To study diseases of the heart and/or blood vessels. Eligibility: People age 2 and older who may have genetic disease affecting the heart and/or blood vessels Their relatives Healthy volunteers Design: Participants will be screened with a medical history, physical exams, and imaging tests. Participants may have a few visits or visits for 2 weeks or more. This will depend on their age and disease status. Visits may include: Photographs of the face and body Heart tests Samples taken of blood, urine, saliva, skin, and/or tissue Scans. For some, a dye may be injected into a vein. A six-minute walk test Lung tests. For some, participants will blow into a tube. For others, they will breathe in a gas from a mask, have a small injection, then have a scan. Stress tests while walking on a treadmill or riding a stationary bike Ultrasound of veins and arteries Devices outside the body testing the stiffness and function of arteries Eye exam and eye tests. For some, a dye may be injected in a vein. Blood pressure tests Measurements of blood flow under the skin and in the arms and fingernail blood vessels Devices outside the body testing flexibility of the blood vessels and skin, and skin temperature
CONDITIONS
Official Title
Vascular Disease Discovery Protocol
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participants must be between 2 and 100 years old
- Pregnant women with known or suspected vascular disease pathology who have been referred or become pregnant during the study
- Unaffected related pregnant women (including spouses/partners) for cord blood and tissue collection only at delivery
You will not qualify if you...
- Healthy volunteers unable to give informed consent
- Healthy volunteers who decline blood draws, tissue studies, or sample storage for future research
- Cognitively impaired individuals who are not affected by vascular disease
- Cognitively impaired individuals not related to affected subjects
- Unaffected unrelated pregnant women
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
National Institutes of Health Clinical Center
Bethesda, Maryland, United States, 20892
Actively Recruiting
Research Team
W
William R Whalen, C.R.N.P.
CONTACT
M
Manfred Boehm, 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
3
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