Registry of cardiovascular complications in people living with HIV

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The RECOVIH registry is an observational project that collects data from adults living with HIV who have additional cardiovascular risk factors and undergo cardiac examinations at the Cardiac Center of Saint Antoine Hospital. This registry aims to evaluate echocardiographic, coronarographic, and blood pressure abnormalities in this population. By maintaining anonymized data, the registry seeks to improve patient care through better risk stratification and understanding of the relationship between HIV and cardiovascular diseases. The findings from this registry may also contribute to research on optimal cardiac care for individuals living with HIV.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* 18 years of age or older
* Known HIV-1 seropositivity for minimum of six months (confirmed by Elisa and Western Blot)
* Underwent complete cardiac examination (echocardiography, ischemia test, ambulatory blood pressure monitoring) between 2005 and 2010 at the Cardiac Center in the Saint Antoine University Hospital in Paris, France
* Presenting a minimum of two cardiovascular risk factors (HIV and a minimum of one other) according to the AFFSSAPS 2005 and Morlat Report 2013.
* Willing and able to give informed consent to participate in the study

Exclusion Criteria :

* Refusal to give or sign informed consent
* Not associated with a social security regime (no health insurance)

Where it's running

• Division of Cardiology, Saint Antoine University Hospital
  Paris, France Recruiting

Study contacts

• Study coordinator: Franck Boccara, MD, PhD
• Email: franck.boccara@aphp.fr
• Phone: +0033 (0) 1 49 28 20 00

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.