ClinicalTrials.gg
RecruitingNCT03795376Updated Jan 15, 2026

Dat'Aids Prevention

An observational study in HIV Prevention, sponsored by DatAids. Recruiting at 31 sites in 3 countries. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-01-15.

Sponsored by DatAids · Observational

From the registry’s dates

  • Started Jan 2019; still recruiting 7 years 10 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
6,500
Ages
18 Years and older
Sex
All
01

Study summary

DatAIDS prevention is a cohort study of HIV prevention in over 23 HIV sites in France including overseas, aiming to describe HIV prevention in every aspect including HIV screening, STI and hepatitis screening, post-exposure prophylaxis and pre-exposure prophylaxis

02

Conditions studied

  • HIV Prevention
03

In context

Lead sponsor

DatAids is the lead sponsor of 2 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

All persons attending for HIV prevention and seeking care at 23 centers using NADIS are included in the Dataids Prevention cohort after receiving oral information and giving written consent. NADIS is an electronic medical record (EMR) for HIV infection (and Hepatitis B virus (HBV), Hepatitis C virus (HCV), STI) and HIV prevention in French public hospitals.

The Dataids Prevention study recruits persons HIV- and above the age of 18 years.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Male and female over 18 years old,
  • negative
  • Attending for :
  • HIV screening
  • Hepatitis screening
  • STI screening / treatment
  • Blood, body fluid or sexual exposure
  • Post-exposure prophylaxis
  • Pre-exposure prophylaxis
  • Signed consent

Exclusion criteria

Exclusion Criteria:

  • -infection
  • Refusal to participate
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
6,500 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Number of patients enrolled for HIV prevention in the cohort

    Demographics, risk factors clinical and biological characteristics, treatment of patients enrolled for HIV prevention in the cohort

    Time frame: From date of enrollment, through study completion, an average of 1 year

Secondary outcomes

  1. Proportion of persons enrolled for pre-exposure prophylaxis in the cohort

    Demographics, risk factors clinical and biological characteristics, treatment of patients attending for pre-exposure prophylaxis in the cohort

    Time frame: From date of enrollment, through study completion, an average of 1 year

  2. Proportion of persons enrolled for post-exposure prophylaxis in the cohort

    Demographics, risk factors clinical and biological characteristics, treatment of patients attending for post-exposure prophylaxis in the cohort

    Time frame: From date of enrollment, through study completion, an average of 1 year

  3. Proportion of persons enrolled for hepatitis screening in the cohort

    Demographics, risk factors clinical and biological characteristics, treatment of patients attending for hepatitis screening in the cohort

    Time frame: From date of enrollment, through study completion, an average of 1 year

  4. Proportion of persons enrolled for pre-exposure prophylaxis in the cohort according to national French guidelines

    Adequation between prevention practices and guidelines

    Time frame: From date of enrollment, through study completion, an average of 1 year

  5. Proportion of persons enrolled for post-exposure prophylaxis in the cohort according to national French guidelines

    Adequation between prevention practices and guidelines

    Time frame: From date of enrollment, through study completion, an average of 1 year

  6. Incidence of STIs

    Time frame: From date of enrollment, through study completion, an average of 1 year

  7. Incidence of hepatitis

    Time frame: From date of enrollment, through study completion, an average of 1 year

07

Study locations

31 of 31 sites recruiting
  • Hôpital Nord Franche Comté
    Belfort, France
    Recruiting
    • Vincent GENDRIN · Contact
    • Vincent GENDRIN · Principal investigator
  • CHU Besançon - Hôpital Jean Minjoz
    Besançon, France
    Recruiting
    • Catherine CHIROUZE · Contact
    • Catherine CHIROUZE · Principal investigator
  • CHRU Brest
    Brest, France
    Recruiting
    • Sylvain JAFFUEL · Contact
    • Sylvain JAFFUEL · Principal investigator
  • CHU Clermont-Ferrand - Hôpital Gabriel-Montpied
    Clermont-Ferrand, France
    Recruiting
    • Christine JACOMET · Contact
    • Christine JACOMET · Principal investigator
  • CHD Vendée
    La Roche-sur-Yon, France
    Recruiting
    • Dominique MERRIEN · Contact
    • Dominique MERRIEN · Principal investigator
  • Hôpital Bicêtre - Assistance Publique des Hôpitaux de Paris
    Le Kremlin-Bicêtre, France
    Recruiting
    • Antoine CHERET · Contact
    • Antoine CHERET · Principal investigator
  • CHU Limoges
    Limoges, France
    Recruiting
    • Claire GENET · Contact
    • Claire GENET · Principal investigator
  • Hôpital de la Croix-Rousse - Hospices Civils de Lyon
    Lyon, France
    Recruiting
    • Dulce ALFAIATE · Contact
    • Dulce ALFAIATE · Principal investigator
  • Hôpital Sainte Marguerite - Assistance Publique des Hôpitaux de Marseille
    Marseille, France
    Recruiting
    • Sylvie BREGIGEON-RONOT · Contact
    • Sylvie BREGIGEON-RONOT · Principal investigator
  • IHU - Assistance Publique des Hôpitaux de Marseille
    Marseille, France
    Recruiting
    • Amélie MENARD · Contact
    • Amélie MENARD · Principal investigator
  • CHR Metz-Thionville
    Metz, France
    Recruiting
    • Céline ROBERT · Contact
    • Céline ROBERT · Principal investigator
  • Hôpital Gui de Chauliac
    Montpellier, France
    Recruiting
    • Alain MAKINSON · Contact
    • Alain MAKINSON · Principal investigator
  • CHU Nancy - Hôpital Brabois
    Nancy, France
    Recruiting
    • Benjamin LEFEVRE · Contact
    • Benjamin LEFEVRE · Principal investigator
  • CHU Nantes - Hôtel-Dieu
    Nantes, France
    Recruiting
    • Clotilde ALLAVENA · Contact
    • Clotilde ALLAVENA · Principal investigator
  • CHU Nice - Hôpital l'Archet
    Nice, France
    Recruiting
    • Pascal PUGLIESE · Contact
    • Pascal PUGLIESE · Principal investigator
  • CH Nîmes
    Nîmes, France
    Recruiting
    • Paul LOUBET · Contact
    • Paul LOUBET · Principal investigator
  • CHR Orléans
    Orléans, France
    Recruiting
    • Laurent HOCQUELOUX · Contact
    • Laurent HOCQUELOUX · Principal investigator
  • Groupe Hospitalier Pitié Salpêtrière - Assistance Publique des Hôpitaux de Paris
    Paris, France
    Recruiting
    • Christine KATLAMA · Contact
    • Christine KATLAMA · Principal investigator
  • Hôpital Bichat - Assistance Publique des Hôpitaux de Paris
    Paris, France
    Recruiting
    • Yazdan YAZDANPANAH · Contact
    • Yazdan YAZDANPANAH · Principal investigator
  • Hôpital Necker-Pasteur - Assistance Publique des Hôpitaux de Paris
    Paris, France
    Recruiting
    • Claudine DUVIVIER · Contact
    • Claudine DUVIVIER · Principal investigator
  • Centre Hospitalier de Cornouaille
    Quimper, France
    Recruiting
    • Nolwenn HALL · Contact
    • Nolwenn HALL · Principal investigator
  • CHU Reims - Hôpital Robert Debré
    Reims, France
    Recruiting
    • Firouze BANISADR · Contact
    • Firouze BANISADR · Principal investigator
  • CHU Rennes - Hôpital Pontchaillou
    Rennes, France
    Recruiting
    • Cédric ARVIEUX · Contact
    • Cédric ARVIEUX · Principal investigator
  • CHU Rouen
    Rouen, France
    Recruiting
    • Manuel ETIENNE · Contact
    • Manuel ETIENNE · Principal investigator
  • CHU St Etienne - Hôpital Nord
    Saint-Etienne, France
    Recruiting
    • Amandine GAGNEUX-BRUNON · Contact
    • Amandine GAGNEUX-BRUNON · Principal investigator
  • CHU Strasbourg - Hôpital Civil
    Strasbourg, France
    Recruiting
    • Axel URSENBACH · Contact
    • Axel URSENBACH · Principal investigator
  • CHU Toulouse - Hôpital Purpan
    Toulouse, France
    Recruiting
    • Pierre DELOBEL · Contact
    • Pierre DELOBEL · Principal investigator
  • CHU Tourcoing - Hôpital Guy Chatiliez
    Tourcoing, France
    Recruiting
    • Olivier ROBINEAU · Contact
    • Olivier ROBINEAU · Principal investigator
  • CH Bretagne-Atlantique
    Vannes, France
    Recruiting
    • Grégory CORVAISIER · Contact
    • Grégory CORVAISIER · Principal investigator
  • CHU de Guadeloupe
    Pointe-à-Pitre, Guadeloupe
    Recruiting
    • Isabelle LAMAURY · Contact
    • Isabelle LAMAURY · Principal investigator
  • CHU de Martinique
    Fort-de-France, Martinique
    Recruiting
    • André CABIE · Contact
    • André CABIE · Principal investigator
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Jan 2019 (actual). Primary completion is estimated for Jan 2030, 132 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Dec 21, 2018
First posted
Jan 7, 2019
StartActual
Jan 1, 2019
Primary completionEst.
Jan 1, 2030
CompletionEst.
Jan 1, 2030
Last update
Jan 15, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jan 15, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03795376
Lead sponsor
DatAids
Responsible party
Sponsor
First posted
Jan 7, 2019
Start date
Jan 1, 2019
Primary completion
Jan 1, 2030 (estimated)
Completion
Jan 1, 2030 (estimated)
Last update
Jan 15, 2026

Study contacts

Pascal Pugliese, MD
Contact
pugliese.p@chu-nice.fr
0033492035802
Solène Secher
Contact
dpo@dataids.org
Pascal PUGLIESE, MD
principal investigator · Centre Hospitalier Universitaire de Nice
André CABIE, MD-PhD
principal investigator · Centre Hospitalier Universitaire de Martinique

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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