HIV Primary Infection
Conditions
Keywords
TUBERCULOSIS IN HIV
Brief summary
The Fujifilm SILVAMP TB LAM (FujiLAM; Fujifilm, Tokyo, Japan) is a novel (not commercialized) urine based point-of-care assay to diagnose TB in HIV-positive patients. A first study using urine frozen samples has reported a higher sensitivity of this test over the currently commercialised Alere Determine TB LAM Ag assay (AlereLAM).
Detailed description
The study aims to assess the performance of a new test called the Fujifilm SILVAMP TB LAM or simply the Fuji-LAM test. The Fuji-LAM test is a test that can be done on urine to look for specific proteins that are produced by the bacteria that causes tuberculosis. This test offers an advantage over the tests that are based on phlegm because most patients can produce urine for testing even when they are very sick. Additionally, this test does not require a complex laboratory set up and it can therefore be used by health workers as they interact with the patient. This study will also look at how the new test compares with an existing test AlereLAM - that is based on similar technology. Initial laboratory-based studies conducted on frozen urine samples show that the new test has better performance than the existing test. This study is different from the first studies because it is being conducted in real life settings rather than in a laboratory. The study will be conducted at the Homa Bay County Hospital in Kenya. Individuals living with HIV with and without signs and symptoms of TB will be invited to take part. Individuals who agree to participate will be seen by the health workers in the study and will provide samples for testing using the FujiLAM test and other standard tests used to investigate individuals for suspected tuberculosis. Investigators are also conducting similar studies in other African countries including Uganda, Mozambique and South Africa. This will enable investigators to assess the performance of the test in diverse settings.
Interventions
DEVICEFUJILAM KIT
Urine based test to detect LAM
Sponsors
Epicentre
Médecins Sans Frontières, Kenya
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE
Masking description
We are not blinding the two arms
Intervention model description
GROUP 1\_ TB SYMPTOMS GROUP2\_ ADVANCED HIV WITH NO TB SYMPTOMS
Eligibility
Sex/Gender
ALL
Age
15 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* 15 years of age or older * HIV-positive Group 1: At least one symptom of TB Group 2: * Advanced HIV disease (CD4 count less than 200cell/µl or clinical stage III/IV) * No signs and symptoms of TB * Signature of the informed consent
Exclusion criteria
* Intake of anti-tuberculosis drugs for more than 5 days in the month prior to the consultation except preventive TB treatment. * Decline to sign informed consent.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| To investigate the diagnostic performance of FujiLAM in ambulatory HIV positive patients. | 12 months | Proportion of patients with a positive FujiLAM result among patients with microbiologically confirmed TB in ambulatory HIV-positive patients with signs and symptoms of TB (Group 1) and Diagnostic performance of FujiLAM test to detect tuberculosis in HIV-positive patients in Kenya - Protocol v2.3 14 in ambulatory HIV-positive patients with advanced HIV disease and no signs and symptoms of TB (Group 2). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| To assess the sensitivity of FujiLAM at different levels of CD4 count. | 12 months | * Proportion of patients with a positive FujiLAM result among patients with probable TB or microbiologically confirmed TB in ambulatory HIV-positive patients with signs and symptoms of TB (Group 1) and in ambulatory HIV-positive patients with advanced HIV disease and no signs and symptoms of TB (Group 2). * Proportion of patients with a positive FujiLAM result among patients with microbiologically confirmed TB and among patients with probable TB or microbiologically confirmed TB by level CD4. * Proportion of patients with a positive AlereLAM among patients with microbiologically confirmed * TB and among patients with probable TB or microbiologically confirmed TB by level of CD4. |
Contacts
Primary ContactHELENA DR Coordinating Principal Investigator, PhD
Backup ContactSTEPHEN DR Site Principal Investigator, MPH
Outcome results
None listed