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Early Identification and Treatment of Early HIV Infection in Côte d'Ivoire

Research Platform Early Identification and Treatment of Early HIV Infection in Côte d'Ivoire

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01917175
Acronym
PRECO-CI
Enrollment
511
Registered
2013-08-06
Start date
1997-06-30
Completion date
2018-09-30
Last updated
2021-06-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV Infection

Keywords

HIV, Cohort, Early HIV infection, Côte d'Ivoire, Disease progression

Brief summary

Set-up of a biobank for patients with an estimated date of infection seroconverters: store plasma and cells samples at initial contact and during follow-up for future analysis and analysis in international collaborative cohort seroconverters.

Interventions

None listed

Sponsors

ANRS, Emerging Infectious Diseases
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients included in the last Primo-CI ANRS 1220 protocol * All HIV infected individuals diagnosed during a blood donation with an estimated date of HIV seroconversion that will respect the following criteria: (i) age ≥18 (ii) HIV-1 or HIV-1+2 infected, (iii) HIV-seronegative at the preceding donation; (iv) who returned to the clinic to be informed of their HIV test result (v) with an HIV serology confirmed with two specific tests in two different laboratories (vi) who have never received ART for curative purpose * informed on study objectives and have a signed informed consent.

Exclusion criteria

* Patient living outside of Abidjan

Design outcomes

Primary

MeasureTime frameDescription
Natural history of HIV infection in Sub-Saharan Africa12 months after ART initiationPlasmatic HIV viral load and CD4 measured every six months and incidence of morbidity events associated with AIDS

Secondary

MeasureTime frameDescription
Evolution of markers of HIV infection and immunity12 months after ART initiationCD4 count, immune activation, plasma HIV-RNA intracellular, HIV-DNA
Viral genetic diversity descriptionInclusion (J0)biomolecular analysis of HIV-1
Primary resistance to antiretroviral treatmentInclusion (J0)Frequency of primary resistance to antiretroviral treatment (genotyping)
Estimate the probability of disease progression after HIV seroconversion12 months after ART initiationDisease progression will be estimated with CD4 cell loss and time from seroconversion to clinical AIDS, death and antiretroviral therapy initiation
Incidence of pregnancies12 months after ART initiationOccurence of pregnancies
T lymphocytes activation and evolution in seroconvertersInclusionDefine parameters of activation of T lymphocytes and their evolution since primo-infection among individuals recently infected in West Africa; Expression of markers CD38, HLA-DR, CD28 and CD127 on CD4 and CD8 T cells by flux cytometry
Metabolic and lipodystrophic disorders12 months after ART initiationMetabolic analysis (Total Cholesterol, HDL and LDL, Triglycerides) and lipodystrophia measurements

Countries

Côte d’Ivoire

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026