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HIV Patients Cohort

Constitution of an Open Monocentric Cohort of HIV Infected Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02203006
Acronym
OVIHD
Enrollment
1613
Registered
2014-07-29
Start date
2011-10-19
Completion date
2030-11-19
Last updated
2026-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients Affected by the HIV

Keywords

HIV,, infection,, cohort

Brief summary

The purpose of this study is to improve our knowledge concerning HIV infection, treated or not, in the current conditions of care to optimize it.

Detailed description

Since the arrival of highly active tritherapies, HIV infection became mainly an ambulatory chronic pathology centred on a long term care taking into account the complication of long-term treatment as well as the arisen of new problem bound to a prolonged survival and ageing. So the care is more and more in a prevention and screening approach with in particular the care of metabolic and cardiovascular complication due to antiretroviral treatment. As a reorganization of the coverage of the HIV infected people take place on the Hotel Dieu Hospital it thus seems important to double this care optimization with a clinical research side. This will be done in constituting an HIV patient cohort including a blood sample collection to contribute to the vigilance of the complication to due the infection. Our ultimate objective is to optimize the selection of the treatment. It is important to do it to be able to have, on many years duration, precise clinical information and biological sample allowing to realize later some assay and analyse the influence of some genetic markers.

Interventions

BIOLOGICALOVIHD

7 ml of blood will be taken during a follow-up consultation and kept in a biological collection. Clinical data will be collected in a database.

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER
URC-CIC Paris Descartes Necker Cochin
CollaboratorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Aged ≥18 years old, * Patients with an HIV infection * patients having given their written informed consent.

Design outcomes

Primary

MeasureTime frameDescription
HIV infection10 yearsThe HIV cohort will be constituted in collecting cardiovascular, neurological clinical data and medical past history (in case of women patient)

Secondary

MeasureTime frameDescription
Comorbidity and complication in HIV infected patients10 yearsThe HIV cohort will be constituted in collecting cardiovascular, neurological clinical data and medical past history (in case of women patient)
efficiency of the current antiretroviral therapeutic diets10 yearsThe HIV cohort will be constituted in collecting cardiovascular, neurological clinical data and medical past history (in case of women patient)
Blood sample collection10 yearsTo put in relation the clinical-biological relevant biological or genetic data of the follow-up a blood sample will be constituted. 7 ml will be taken to each patient and kept in a collection

Countries

France

Contacts

STUDY_DIRECTORJean-Marc Tréluyer, MD, PhD

Assistance Publique - Hôpitaux de Paris

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 7, 2026