Clinical trial Recruiting at 39 sites Observational Ages 18 and up

Long-term monitoring of HIV-infected patients in France

Official title: Dataids Prospective Observational Cohort on Quality of Care of French HIV Infected Patients

Run by DatAids · NCT02898987 · Data updated 2026-11-12

This study is collecting health information from over 30,000 people with HIV in France to see how their treatment and care change over time and how well their medications are working.

More HIV trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment30000 (estimated)
SponsorDatAids
Academic / other
Locations39 sites (Belfort and 38 other locations)
StatusRecruiting
StartedJanuary 2016
Main results expectedJanuary 2030
Study endsJanuary 2030
Registry record updatedFebruary 20, 2026
Trial IDNCT02898987 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are HIV-1 infected patients of any age who are seeking care at participating HIV centers in France.

Probably not a fit

Patients under 18 years of age or those unable to provide written informed consent will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to collect and analyze clinical, laboratory, and therapeutic data from over 30,000 HIV-infected patients across 15 HIV centers in France. The study focuses on understanding the clinical practice and changes in the management of HIV and related co-infections over time. It evaluates the effectiveness of antiretroviral therapy (ART) and monitors the treatment outcomes for hepatitis C virus (HCV) among the cohort. Data is collected as part of routine care during scheduled outpatient visits, regardless of patients' CD4 cell count or ART status.

Why it matters

Potential benefit: If successful, this study could enhance the understanding of HIV management and improve treatment strategies for patients.

How similar studies have gone: Other studies have successfully utilized similar cohort approaches to monitor HIV and its comorbidities, indicating a strong precedent for this methodology.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* HIV-1 infected patients regardless of CD4 cell count and antiretroviral therapy status

Exclusion Criteria:

* Patients under 18 years of age
* Patients without written informed consent

Where it's running

  • Hôpital Nord Franche Comté
    Belfort, France
    Recruiting
  • CHU Besançon - Hôpital Jean Minjoz
    Besançon, France
    Recruiting
  • CHRU Brest
    Brest, France
    Recruiting
  • Centre Hospitalier de Brive
    Brive-la-Gaillarde, France
    Recruiting
  • CHU Clermont-Ferrand - Hôpital Gabriel-Montpied
    Clermont-Ferrand, France
    Recruiting
  • Chic
    Créteil, France
    Recruiting
Show 33 more locations
  • Faye-l'Abbesse, France Recruiting
  • CHD Vendée
    La Roche-sur-Yon, France
    Recruiting
  • Centre Hospitalier de La Rochelle
    La Rochelle, France
    Recruiting
  • Hôpital Bicêtre - Assistance Publique des Hôpitaux de Paris
    Le Kremlin-Bicêtre, France
    Recruiting
  • CHU Limoges
    Limoges, France
    Recruiting
  • Hôpital de la Croix-Rousse - Hospices Civils de Lyon
    Lyon, France
    Recruiting
  • Hôpital Sainte Marguerite - Assistance Publique des Hôpitaux de Marseille
    Marseille, France
    Recruiting
  • IHU - Assistance Publique des Hôpitaux de Marseille
    Marseille, France
    Recruiting
  • CHR Metz-Thionville
    Metz, France
    Recruiting
  • Hôpital Gui de Chauliac
    Montpellier, France
    Recruiting
  • CHU Nancy - Hôpital Brabois
    Nancy, France
    Recruiting
  • CHU Nantes - Hôtel-Dieu
    Nantes, France
    Recruiting
  • CHU Nice
    Nice, France
    Recruiting
  • Centre Hospitalier de Niort
    Niort, France
    Recruiting
  • CH Nîmes
    Nîmes, France
    Recruiting
  • CHR Orléans
    Orléans, France
    Recruiting
  • Groupe Hospitalier Pitié Salpêtrière - Assistance Publique des Hôpitaux de Paris
    Paris, France
    Recruiting
  • Hôpital Bichat - Assistance Publique des Hôpitaux de Paris
    Paris, France
    Recruiting
  • Hôpital Necker-Pasteur - Assistance Publique des Hôpitaux de Paris
    Paris, France
    Recruiting
  • Centre Hospitalier de Cornouaille
    Quimper, France
    Recruiting
  • CHU Reims - Hôpital Robert Debré
    Reims, France
    Recruiting
  • CHU Rennes - Hôpital Pontchaillou
    Rennes, France
    Recruiting
  • CH Rochefort
    Rochefort, France
    Recruiting
  • CHU Rouen
    Rouen, France
    Recruiting
  • CHU St Etienne - Hôpital Nord
    Saint-Etienne, France
    Recruiting
  • CHU Strasbourg - Hôpital Civil
    Strasbourg, France
    Recruiting
  • CHU Toulouse - Hôpital Purpan
    Toulouse, France
    Recruiting
  • CHU Tourcoing - Hôpital Guy Chatiliez
    Tourcoing, France
    Recruiting
  • CH Troyes
    Troyes, France
    Recruiting
  • CH Bretagne-Atlantique
    Vannes, France
    Recruiting
  • Chiv
    Villeneuve-Saint-Georges, France
    Recruiting
  • CHU de Guadeloupe
    Pointe-à-Pitre, Guadeloupe
    Recruiting
  • CHU de Martinique
    Fort-de-France, Martinique
    Recruiting

Study contacts

  • Principal investigator: Pascal PUGLIESE, MD — Centre Hospitalier Universitaire de Nice
  • Study coordinator: Pascal Pugliese, MD
  • Email: pugliese.p@chu-nice.fr
  • Phone: 0033492035802

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
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Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.