In this prospective cohort study the investigators will assess the prevalence and incidence of a broad range of age-related co-morbidities and their (known) risk factor among HIV-patients and HIV-negative controls. HIV might cause premature onset or accelerated aging and could therefore result in an increase of age-related comorbidities when compared with controls.
Eligibility
Sex
ALL
Min age
45 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria:
* For the HIV-positive patients: HIV-1 infection and aged 45 years and above
* For the HIV-negative controls: HIV-uninfected and aged 45 years and above
Exclusion Criteria:
* None
Primary outcome measure(s)
The prevalence of comorbidities, organ system dysfunction and their risk factors at time of enrolment — at enrolment and after every 2 years follow up. The Ethics Committee has approved for the study to continue without a set end-date, depending on continued funding. To assess the prevalence and incidence of comorbidities, organ system dysfunction and their risk factors over two years of follow-up in a cohort of HIV-infected individuals (mostly on antiretroviral therapy) and in a cohort of comparable but uninfected controls
The incidence of comorbidities, organ system dysfunction and their risk factors after two years of follow up — After every 2 years of follow up.The Ethics Committee has approved for the study to continue without a set end-date, depending on continued funding. To assess the incidence of comorbidities, organ system dysfunction and their risk factors after tow years of follow up in a cohort of HIV-infected individuals (mostly on antiretroviral therapy) in comparison to that of a cohort of comparable but uninfected controls
Trial sites (2)
Facility
City
Region
Status
Public Health Service Amsterdam
Amsterdam
Netherlands
Academic Medical Center
Amsterdam
Netherlands
More Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) trials in the Netherlands
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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