Skip to content

Cohorte Nationale VIH-2

Cohorte ANRS CO5 Cohorte Nationale VIH2

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04658329
Acronym
ANRS CO VIH2
Enrollment
1185
Registered
2020-12-08
Start date
1994-01-01
Completion date
2022-09-30
Last updated
2020-12-08

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

Conditions

HIV-2 Infection

Keywords

virus, HIV, cohort

Brief summary

The HIV2 study is an open cohort of prospective, multicentric, national observation. The main objective is to study HIV-2 infection in adult patients followed in France.

Detailed description

The secondary objectives are : * Describe the epidemiological and clinical characteristics of participants infected with HIV-2, and the immuno-virological characteristics of the infection. * To study the clinical and immunological progression of HIV-2 infection and the prognostic factors of this evolution. * Study the response to antiretroviral treatment (clinical, immuno-virological) and contribute to the identification of the antiretroviral strategies and combinations most suited to the particularities of the infection. * Allow an evaluation of the care practices of participants followed in French hospitals * Provide a bank of clinical-biological data and samples allowing the performance of virological and / or immunological studies on HIV-2 infection. The follow-up of the participants is different according to the therapeutic status of the participants, naive of antiretroviral treatment or already treated with antiretrovirals.

Interventions

Study the response to antiretroviral treatment (clinical, immuno-virological) and contribute to the identification of the antiretroviral strategies and combinations most suited to the particularities of the infection.

Sponsors

ANRS, Emerging Infectious Diseases
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* HIV-2 infection only, diagnosed by ELISA, confirmed by Western-Blot test, * Follow-up in consultation or hospitalization in one of the investigating centers, * Age greater than or equal to 18 years, * Prolonged follow-up possible, residence in France planned for at least one year, * Consent to participate, * Long-term medical care possible for the participant, or by medical aid (AME), or declaration of obtaining AME at the time of inclusion.

Exclusion criteria

* HIV-1 infection * Double HIV-1 + HIV-2 seropositivity

Design outcomes

Primary

MeasureTime frame
Study HIV-2 infection rate in adult patients followed in FranceAt the baseline

Secondary

MeasureTime frameDescription
The epidemiological parameters and progression of patients infected with HIV-2 evaluate by a questionnaireUp to 25 yearsEvery 6 months
The rate of immuno-virological charge of the infection evaluate by serology samplesUp to 25 yearsEvery 6 months
The clinical progression of patients infected HIV-2 evaluate by samples: biological examinationsUp to 25 yearsEvery 6 months
Pourcentage of response to antiretroviral treatment evaluate by serology samplesUp to 25 years
Pourcentage of good management practices of patients followed in French hospitals evaluate by resultsUp to 25 yearsDuring the procedure
Pourcentage of patient with HIV-2Up to 25 yearsThe prognostic factors of patient evolution are evaluate by biological samples

Countries

France

Contacts

Primary ContactSophie Matheron, Pr, MD
sophie.matheron@aphp.fr01 40 25 72 39
Backup ContactJulie Longobardi
julie.longobardi@u-bordeaux.fr05 57 57 48 12

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026