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Clinical Trials/NCT02203006
NCT02203006
Active, not recruiting
Not Applicable

Constitution of an Open Monocentric Cohort of HIV Infected Patients

Assistance Publique - Hôpitaux de Paris1 site in 1 country1,613 target enrollmentOctober 19, 2011
InterventionsOVIHD

Overview

Phase
Not Applicable
Intervention
OVIHD
Conditions
Patients Affected by the HIV
Sponsor
Assistance Publique - Hôpitaux de Paris
Enrollment
1613
Locations
1
Primary Endpoint
HIV infection
Status
Active, not recruiting
Last Updated
5 months ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
October 19, 2011
End Date
April 1, 2031
Last Updated
5 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

  • Not provided

Arms & Interventions

OVIHD

Cohort and a blood sample collection will be done with data and blood of HIV infected patients

Intervention: OVIHD

Outcomes

Primary Outcomes

HIV infection

Time Frame: 10 years

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

Secondary Outcomes

  • Comorbidity and complication in HIV infected patients(10 years)
  • efficiency of the current antiretroviral therapeutic diets(10 years)
  • Blood sample collection(10 years)

Study Sites (1)

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