Nice HIV Cohort Follow-Up
Official title: Nice Human Immunodeficiency Virus (HIV) Cohort
Run by Centre Hospitalier Universitaire de Nice · NCT03690063 · Data updated 2026-11-12
This project follows people with HIV who have scheduled outpatient visits to see how their health changes over time using routine medical records.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 2000 (estimated) |
| Sponsor | Centre Hospitalier Universitaire de Nice Academic / other |
| Locations | 1 site (Nice) |
| Status | Recruiting |
| Started | January 1, 1996 |
| Main results expected | January 30, 1996 |
| Study ends | June 25, 2027 |
| Registry record updated | June 29, 2026 |
| Trial ID | NCT03690063 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with HIV who have a scheduled outpatient visit at CHU de Nice and consent to have their routine care data used for the cohort.
✕Probably not a fit
Patients not engaged in routine outpatient visits or who do not consent to data use may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational cohort uses the NADIS computerized medical record to track outcomes of people living with HIV who come in for regular outpatient visits. It builds on historical HIV databases and collects data from patients during standard care visits. The aim is to understand long-term patterns in health, treatment, and outcomes without assigning any new interventions. Data are drawn from existing medical records and follow-up is based on standard clinical appointments.
Why it matters
Potential benefit: If successful, the cohort could provide insights into long-term HIV care and inform improvements in management strategies.
How similar studies have gone: Previous HIV-focused databases and cohorts have contributed meaningful knowledge using similar follow-up approaches.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Enrol consecutive patients with a scheduled visit in the outpatient clinic (regardless of CD4 cell count and ART status). Exclusion Criteria: \-
Where it's running
-
CHU de Nice
Nice, France Recruiting
Study contacts
- Study coordinator: Christian PRADIER, Pr
- Email: pradier.c@chu-nice.fr
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.