Study of Entry and Continuation in Care for People Living With HIV in French Guiana - Trial NCT05354934
Access comprehensive clinical trial information for NCT05354934 through Pure Global AI's free database. This phase not specified trial is sponsored by Centre Hospitalier de Cayenne and is currently Recruiting. The study focuses on Human Immunodeficiency Virus. Target enrollment is 300 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.
Study Focus
Sponsor & Location
Centre Hospitalier de Cayenne
Timeline & Enrollment
N/A
Mar 23, 2022
Jun 23, 2023
Primary Outcome
Identifying factors associated with loss of sight for more than 12 months among people living with HIV in Guyana
Summary
Research Involving the Non-Interventional Human Subject (RIPH category 3).
 Non-interventional, cross-sectional, multicentre, descriptive and analytical epidemiological
 study.
 
 A cross-sectional, pseudo-anonymous questionnaire focusing on entry and retention in care
 will be administered to a sample of PLHIV presenting for consultation in one of the GHT
 hospitals over a 12-month period.
 
 A sample of 300 PHAs is envisaged to have sufficient power to highlight the main factors
 associated with periods of loss of sight.
 
 Main objective:
 
 - To identify factors associated with loss of sight for more than 12 months among people
 living with HIV in Guyana
 
 Secondary objectives:
 
 - To identify factors associated with a delay in the introduction of ARVs among PLHIV in
 Guyana
 
 - To describe the perception of the quality of the announcement of the diagnosis of HIV
 
 - To describe the difficulties encountered by PLHIV during their hospital follow-up in
 French Guyana
 
 - To assess the perceived stigma associated with HIV and its consequences in daily life
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT05354934
Non-Device Trial

