Use of Long-Acting Injectable Cabotegravir/Rilpivirine for the Treatment of HIV in Belgium
Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY
This will be a multi-center, single arm observational cohort study with an assessment of patient-reported outcomes (PROs) and of clinical and virologic outcomes. Primary outcome • Evaluate patient perception of, and satisfaction with, long-acting injectable (LAI) cabotegravir/rilpivirine (CAB/RPV) for the treatment of HIV Secondary outcomes • Description of the demographic, HIV-, and non-HIV-related characteristics of participants included in this analysis
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 99
Healthy Volunteers: f
View:
• HIV-1 patients, aged 18 years and above, having received at least 1 dose of LAI CAB/RPV between September 1, 2021, and March 31, 2024.
Locations
Other Locations
Belgium
Saint-Pierre University Hospital
RECRUITING
Brussels
Contact Information
Primary
Rakan Nasreddine, MD
rakan.nasreddine@stpierre-bru.be
+32 2 535 4130
Time Frame
Start Date: 2025-01-13
Estimated Completion Date: 2025-07
Participants
Target number of participants: 600
Related Therapeutic Areas
Sponsors
Leads: Belgian Research on AIDS and HIV Consortium