The objective of the Dataids cohort is to continue a long-term, prospective collection of clinical, laboratory and therapeutic data on a large cohort of HIV infected patients seeking care in 15 HIV centers in France in order : 1. to provide and develop a surveillance system to describe clinical practice and temporal changes in the clinical course of HIV and HIV-related co-infections and co-morbidities in France. 2. to assess the factors associated with the clinical, immunological and virological course of HIV infection and HIV-related co-infections and co-morbidities The specific objectives are as follows * To continue surveillance of HIV infection in France to describe temporal changes * To evaluate the efficacy of ART and factors associated with ART efficacy * To monitor the uptake and outcome of HCV therapy
The Dataids cohort is a prospective observational cohort of 30,000+ patients followed in 15+ HIV centers scattered throughout France. The Dataids cohort is an ongoing collaboration and patients have been enrolled into the study since 2010; the data are collected from the clinics as part of routine care. Included patients should be patients who had a scheduled visit in the outpatient clinic regardless of CD4 cell count, HIV viral load or ART status. For all HIV patients enrolled and under follow up, demographic data, immunological and virological data, serological evidence for infection with hepatitis B virus (HBV), hepatitis C virus (HCV), or syphilis, laboratory, therapeutic and clinical data are collected annually.
Study Type
OBSERVATIONAL
Enrollment
30,000
Hôpital Nord Franche Comté
Belfort, France
RECRUITINGCHU Besançon - Hôpital Jean Minjoz
Besançon, France
RECRUITINGCHRU Brest
Brest, France
RECRUITINGCentre Hospitalier de Brive
Brive-la-Gaillarde, France
Proportion of HIV treated patients with HIV plasma viral load < 50 copies/mL
Time frame: From date of enrollment, through study completion, an average of 6 months
Proportion of HIV/HCV coinfected patients who start treatment with direct acting antivirals agents
Time frame: From date of enrollment, through study completion, an average of 1 year
Proportion of HIV patients according to their antiretroviral status : naive, on treatment, therapeutic stop
Time frame: From date of enrollment, through study completion, an average of 1 year
proportion of HIV/HCV patients with undetectable HCV viral load after treatment with direct acting antivirals agents
Time frame: From date of enrollment, through study completion, an average of 1 year
Proportion of HIV patients with CD4 cells count above 500 /ml
Time frame: From date of enrollment, through study completion, an average of 1 year
Incidence of antiretroviral modification due to simplification or failure
The observational cohort study concept means that Dataids does not collect Adverse Events, Adverse Reactions, Serious Adverse Reactions or Suspected Unexpected Serious Adverse Reactions as defined by pharmacovigilance requirements for marketing authorization holders. However, Dataids often analyses and reports specific clinical events of interest, occasionally related to drug classes, but more regularly with a focus on differences in treatment and care
Time frame: From date of enrollment, through study completion, an average of 1 year
Incidence of aids events among patients enrolled in the cohort study
Time frame: From date of enrollment, through study completion, an average of 1 year
Incidence of non aids events among patients enrolled in the cohort study
Time frame: From date of enrollment, through study completion, an average of 1 year
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CHU Clermont-Ferrand - Hôpital Gabriel-Montpied
Clermont-Ferrand, France
RECRUITINGCHIC
Créteil, France
RECRUITINGUnnamed facility
Faye-l'Abbesse, France
RECRUITINGCHD Vendée
La Roche-sur-Yon, France
RECRUITINGCentre Hospitalier de La Rochelle
La Rochelle, France
RECRUITINGHôpital Bicêtre - Assistance Publique des Hôpitaux de Paris
Le Kremlin-Bicêtre, France
RECRUITING...and 29 more locations