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Taking people in FranceNo phase

Registry following heart health in adults living with HIV

Records heart complications and related data in adults with HIV at one hospital.

Plain-language title generated from the registry record
Registry title: Register of Cardiovascular Complications Among People Living With HIV

Key facts

Where
Paris, FranceSee the site

Where in France

  • Division of Cardiology, Saint Antoine University HospitalParis, FranceTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Saint Antoine University Hospital
Trial code
NCT02453919
Record updated
30 January 2024
Original description
The REgister of cardiovascular COmplications among people living with HIV (RECOVIH) is a single hospital registry of adults living with HIV, with one or more other cardiovascular risk factor, who undergo cardiac examination at the Cardiac Center of the Saint Antoine Hospital.Read full original descriptionShow less

Register of Cardiovascular Complications Among People Living With HIV

The REgister of cardiovascular COmplications among people living with HIV (RECOVIH) is a single hospital registry of adults living with HIV, with one or more other cardiovascular risk factor, who undergo cardiac examination at the Cardiac Center of the Saint Antoine Hospital.

RECOVIH is an observational and prospective, monocentric (institutional) registry, with anonymized cardiac, biochemical and associated data collection.

Inclusion: 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: Refusal to give or sign informed consent; Not associated with a social security regime (no health insurance).

ClinicalTrials.gov NCT02453919