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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05433987
Other study ID # CHC-PI-2022-01
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date July 2022
Est. completion date July 2023

Study information

Verified date June 2022
Source Centre Hospitalier de Cannes Simone Veil
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of the study is to measure the impact on immune activation and inflammatory markers of switching from a triple combination antiretroviral therapy (cART) to a long acting dual therapy in HIV-infected patients


Description:

Patients meeting the inclusion criteria will be offered to participate to the study. In case of acceptance by given their writting consent, 6 ml of blood will be collected for measuring immune activation and inflammatory markers, during the blood test scheduled for the routine follow-up. Six months after cART change, an equal volume of blood will be collected for measuring the same immune activation and inflammatory markers


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date July 2023
Est. primary completion date July 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients agreeing to participate to the study and to collect their data - HIV-1 infected subjects - Patients switching from a stable (at least 6 months) and successful triple cART to a long acting dual cART - Patients older than 18 yrs and regularly followed in Cannes and Nice hospitals - Patients with a healthcare card Exclusion Criteria: - HIV-2 infected subjects - Patients not being on successful and stable cART - Patients having being treated during acute HIV-infection - Patients modifying cART for virological failure - Subjects modifying their treatment for another combination than from a triple cART to a dual cART - Patients modifying cART during the 6 months of follow-up - Patients refusing to participate to the study - Patients included in an interventional study during the 6 months of follwo-up - Patient under juridical procedure

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier de Cannes Simone Veil

Outcome

Type Measure Description Time frame Safety issue
Primary Evolution the trajectory of immune activation and inflammatory markers Assess the trajectory of immune activation and inflammatory markers change at 6 month after modifying cART Baseline and 6 months after modiyfying cART
Secondary Prevalence of patients with successful cART To evaluate prevalence of patients with successful cART (i.e. viral load below 50 copies/ml) 1 month after the switch 1 month, 3 month, 6 month
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