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Implementation Protocol for Rapid Diagnostic Tests for Opportunistic Infections in Reference Centers in Mexico City
In Mexico City, the main cause of mortality among people living with HIV (PLHIV) continues to be opportunistic infections (OIs). Early detection of OIs allows their timely treatment and improves their prognosis. The use of rapid diagnostic tests (RDT) based on antigens of the most frequent causative agents of OIs allows adequate screening of these patients and facilitates decision making at the point of care. Unfortunately, these studies are not widely available in the different PLHIV care centers in the CDMX. We will conduct an open-label, non-inferiority uncontrolled clinical trial to investigate the diagnostic performance of urinary lipoarabinomannan, urinary Histoplasma antigen and serum Cryptococcus antigen in patients presenting for care with advanced HIV in CDMX, supported by rapid cluster of differentiation 4 (CD4) testing with lateral flow technology. Four referral hospitals will participate over 12 months. All patients with diagnosed HIV disease and suspected advanced disease presenting for care at participating centers will be included in the study. An inventory of approximately 1000 RDT will be obtained and distributed among the participating sites. A study coordinator will be hired and will visit each site once a week to collect the study variables and follow up on the included patients. The primary outcome of the study will be the percentage of patients with advanced disease who present with diagnoses made by RDT compared to historical controls of patients diagnosed with OI in 2022 at participating centers by conventional methods. Secondary outcomes will be time to initiation of antiretroviral therapy (ART), time to initiation of OI treatment, and 30-day mortality after HIV diagnosis.
Age
18 - 100 years
Sex
ALL
Healthy Volunteers
No
General Hospital Dr. Manuel Gea Gonzalez
Mexico City, Mexico
National Center of Nutrition and Medical Sciences
Mexico City, Mexico
National Institute of Cancerology
Mexico City, Mexico
National Institute of Respiratory Diseases
Mexico City, Mexico
Start Date
April 1, 2023
Primary Completion Date
March 30, 2024
Completion Date
September 30, 2024
Last Updated
January 17, 2023
211
ESTIMATED participants
Histoplasma Urine Antigen Lateral Flow Antigen test
DIAGNOSTIC_TEST
Cryptococcal Lateral Flow Antigen test
DIAGNOSTIC_TEST
Tuberculosis-lipoarabinomannan Lateral Flow Antigen test
DIAGNOSTIC_TEST
Lead Sponsor
National Institute of Respiratory Diseases, Mexico
Collaborators
NCT05342064
NCT06221488
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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View ClinicalTrials.gov Terms and ConditionsNCT06033807