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Risk of Morbidity, Mortality and Long-term Monitoring of Antiretroviral Treatment in People Living With HIV: The ANRS CO3 Aquitaine Cohort - AquiVIH-NA
HIV infection is now a chronic disease in countries where antiretroviral treatments (ART) are largely available. Long-term follow-up is required to describe and understand the evolution of morbidities and complications as well as new treatments side effects. The main objective of the cohort is to describe and study the evolution of HIV infection in ART-treated individuals.
The survival of people living with HIV (PLHIV) taking antiretroviral therapy (ART) is now close to what is reported in the general population in northern countries. However, PLHIV experience an increased risk of morbidities that the ANRS CO3 Aquitaine Cohort has largely contributed to describe in the last years. Among contributing factors to this excess of morbidity, immune suppression, immune activation, and exposition to cardiovascular and cancer risk factors as well as ageing represent possible intervention targets. Long-term follow-up is required to describe and understand the evolution of morbidities and complications as well as ART side effects. Moreover, the global evaluation of health in PLHIV, including psychiatric, neurologic and social determinants and not only biomedical determinants represents one of the public health challenges of the next decade in the field of HIV infection. The aim of the present study is to study the emerging morbidity occurring during the course of HIV infection in people treated with ART as well as to describe the tolerance and efficacy of new available ART regimens. The follow-up of patients will be performed according to national guidelines. Demographic, clinical, biological and therapeutic data will be captured at each patient's hospital contact according to a standardized questionnaire. All events occurring during the course of clinical management will be prospectively registered in the database according to the ICD 10th revision. A biobank will be collected from every consenting PLHIV at inclusion in the cohort and then every two years.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
service de médecine interne - CH d'Agen
Agen, France
Médecine interne - CH d'Angoulême
Angoulême, France
service de maladies infectieuses - CH de la Côte Basque
Bayonne, France
service de médecine inter et maladies infectieuses - Hopital Saint André
Bordeaux, France
service de médecine interne et maladies infectieuses - Hôpital Saint-André
Bordeaux, France
service de maladies infectieuses et médecine tropicale - Hôpital Pellegrin
Bordeaux, France
service de maladies infectieuses et médecine tropicale - Hôpital Pellegrin
Bordeaux, France
service de maladies infectieuses et médecine tropicale - Hôpital Pellegrin
Bordeaux, France
Service D'Urgences Pédiatriques
Bordeaux, France
médecine interne - CH de Châtellerault
Châtellerault, France
Start Date
July 18, 2017
Primary Completion Date
July 1, 2025
Completion Date
July 1, 2025
Last Updated
February 21, 2025
7,200
ESTIMATED participants
Lead Sponsor
University Hospital, Bordeaux
Collaborators
NCT04142047
NCT06694805
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07428330