Plain-English translation of NCT02453919 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This is a heart health registry — a database that collects information about how HIV affects the heart and blood vessels in adults living with HIV. Researchers and doctors use this registry to understand cardiac (heart) complications in people with HIV and to improve how they care for and protect heart health in this population.
Very little is known about the best way to monitor and treat heart disease in people living with HIV. By gathering heart test results and health information from many patients in one place, doctors hope to identify who is at highest risk for heart problems and develop better ways to prevent and manage them.
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As a participant, you would have already undergone complete heart tests (including heart ultrasound, stress tests, and 24-hour blood pressure monitoring) at the hospital's cardiac center. The registry then collects and stores your heart test results, blood work, and other health information to help doctors better understand heart disease in people with HIV. There are no ongoing visits or treatments required — you are simply allowing your existing cardiac data to be part of this research database.
AI-generated summary from trial data · Jun 9, 2026 · Not medical advice
France
Enrollment target
~800 participants
Started
February 2010
Primary completion
December 2030
Age range
18 Years and older
Last updated on clinicaltrials.gov in January 2024.
Reach out to the team running this trial. Response times vary — some teams are faster than others.
Central contact
Franck Boccara, MD, PhD
Saint Antoine University Hospital
Tell us you're interested and we'll help connect you with the research team. We'll walk you through what to expect first — no email needed to get started.