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Clinical Trials/NCT03690063
NCT03690063RecruitingNot Applicable

Nice Human Immunodeficiency Virus (HIV) Cohort

Centre Hospitalier Universitaire de Nice1 site in 1 country2,000 target enrollmentStarted: January 1, 1996Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
2,000
Locations
1
Primary Endpoint
change of the clinico-biological signs of the patients
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

Historically, the database on the HIV was organized within the framework of the medico-economic file of the human immunodeficiency (DMI-2), introduced jointly by the Direction of Hospitals (Mission AIDS) and the INSERM at the end of the 80s. Today this database is fed via the computerized medical record NADIS. Most part of the research works on the theme of the HIV take support on this database (DAD, EuroAIDS, Neuradapt).

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Enrol consecutive patients with a scheduled visit in the outpatient clinic (regardless of CD4 cell count and ART status).

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

change of the clinico-biological signs of the patients

Time Frame: Each Year during 50 years

change of the clinico-biological values form the start of the study, mesured every year, to the end of the study

Secondary Outcomes

  • number of the various type of adverse events related by type of treatments(Each Year during 50 years)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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