Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
1185 participants
OBSERVATIONAL
1994-01-01
2022-09-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
* 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.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Antiretroviral
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.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
* Double HIV-1 + HIV-2 seropositivity
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
ANRS, Emerging Infectious Diseases
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
François Dabis, Pr, MD
Role: STUDY_DIRECTOR
ANRS, Emerging Infectious Diseases
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Centre hospitalier Victor Dupouy
Argenteuil, , France
Avicenne
Bobigny, , France
Hôpital Saint André
Bordeaux, , France
Service de Medecine Interne Hopital Antoine Beclere
Clamart, , France
Hôpital Louis Mourier
Colombes, , France
Hôpital Sud Francilien
Corbeil-Essonnes, , France
Hôpital Henri Mondor
Créteil, , France
Service de Médecine interne - Centre Hospitalier Intercommunal
Créteil, , France
Hôpital Edouard Herriot
Lyon, , France
Hôpital de La Croix Rousse
Lyon, , France
Centre Hospitalier François Quesnay
Mantes-la-Jolie, , France
Hôpital Gui de Chaudiac
Montpellier, , France
Hôpital de l'Hotel Dieu
Nantes, , France
Hôpital Saint Louis
Paris, , France
Hôpital Saint Antoine
Paris, , France
Hôpital la Pitié Salpétrière
Paris, , France
Service de Medecine Interne Hopital Cochin
Paris, , France
Hôpital Bichat - Claude Bernard
Paris, , France
Hôpital Tenon
Paris, , France
Hôpital Hôtel Dieu
Paris, , France
Hôpital Lariboisière
Paris, , France
Hopital du Kremlin Bicêtre Service de médecine interne
Paris, , France
Centre Hospitalier René Dubos
Pontoise, , France
Hôpital Pontchaillou
Rennes, , France
Hôpital Delafontaine
Saint-Denis, , France
CHI Poissy Saint Germain en Laye
Saint-Germain-en-Laye, , France
Hôpital Bretonneau - Service des Maladies Infectieuses
Tours, , France
Hôpital André Mignot
Versailles, , France
CHI Villeneuve Saint Georges
Villeneuve-Saint-Georges, , France
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Philippe PG GENET, MD
Role: primary
Juliette JG GERBE
Role: backup
Olivier OB BOUCHAUD, PhD
Role: primary
MOHAMED KASSIM MKY YOUSSOUF, MD
Role: backup
Philippe Morlat, Pr
Role: primary
Francois Boue, MD
Role: primary
Emmanuel Mortier, MD
Role: primary
Jean-Daniel Lelievre, MD, PhD
Role: primary
Valérie GARRAIT, MD
Role: primary
Djamila MAKHLOUFI
Role: primary
Laurent COTTE
Role: primary
Ahmed JABBAR
Role: primary
Jacques Reynes
Role: primary
François RAFFI
Role: primary
Jean-Michel Molina, Pr
Role: primary
Marie Caroline Meyohas, Pr
Role: primary
Dominique Salmon, MD
Role: primary
Pialloux Gilles, Pr
Role: primary
Jean-Paul Viard, MD
Role: primary
Agathe Rami, Dr
Role: primary
Cécile Goujard, MD
Role: primary
Laurent BLUM
Role: primary
Cedric Arvieux, Dr
Role: primary
Marie-Aude KHUONG
Role: primary
Yves Welker, MD
Role: primary
Louis Bernard, PH
Role: primary
Alix Greder-Belan, MD
Role: primary
Olivier Patey, MD
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
ANRS CO5 VIH-2
Identifier Type: -
Identifier Source: org_study_id