Diagnostic Performance of a Novel Lipoarabinomannan. (FUJILAM)
Primary Purpose
HIV Primary Infection
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
FUJILAM KIT
Sponsored by
About this trial
This is an interventional diagnostic trial for HIV Primary Infection focused on measuring TUBERCULOSIS IN HIV
Eligibility Criteria
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.
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Ambulatory HIV positive patients
Arm Description
Ambulatory HIV positive patients with signs and symptoms of TB, and Ambulatory HIV positive patients with advanced disease and CD4 less than 200 cell.
Outcomes
Primary Outcome Measures
To investigate the diagnostic performance of FujiLAM in ambulatory HIV positive patients.
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 Outcome Measures
To assess the sensitivity of FujiLAM at different levels of CD4 count.
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.
Full Information
NCT ID
NCT05036694
First Posted
July 8, 2021
Last Updated
August 30, 2021
Sponsor
Médecins Sans Frontières, Kenya
Collaborators
Epicentre
1. Study Identification
Unique Protocol Identification Number
NCT05036694
Brief Title
Diagnostic Performance of a Novel Lipoarabinomannan.
Acronym
FUJILAM
Official Title
Diagnostic Performance of a Novel Lipoarabinomannan Test (FujiLAM) to Detect Tuberculosis in HIV-positive Patients in Kenya
Study Type
Interventional
2. Study Status
Record Verification Date
July 2021
Overall Recruitment Status
Unknown status
Study Start Date
September 2021 (Anticipated)
Primary Completion Date
September 2022 (Anticipated)
Study Completion Date
December 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Médecins Sans Frontières, Kenya
Collaborators
Epicentre
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Primary Infection
Keywords
TUBERCULOSIS IN HIV
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
GROUP 1_ TB SYMPTOMS GROUP2_ ADVANCED HIV WITH NO TB SYMPTOMS
Masking
None (Open Label)
Masking Description
We are not blinding the two arms
Allocation
N/A
Enrollment
550 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Ambulatory HIV positive patients
Arm Type
Other
Arm Description
Ambulatory HIV positive patients with signs and symptoms of TB, and Ambulatory HIV positive patients with advanced disease and CD4 less than 200 cell.
Intervention Type
Device
Intervention Name(s)
FUJILAM KIT
Intervention Description
Urine based test to detect LAM
Primary Outcome Measure Information:
Title
To investigate the diagnostic performance of FujiLAM in ambulatory HIV positive patients.
Description
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).
Time Frame
12 months
Secondary Outcome Measure Information:
Title
To assess the sensitivity of FujiLAM at different levels of CD4 count.
Description
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.
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
HELENA DR Coordinating Principal Investigator, PhD
Phone
+32493837895
Email
Helena.HUERGA@epicentre.msf.org
First Name & Middle Initial & Last Name or Official Title & Degree
STEPHEN DR Site Principal Investigator, MPH
Phone
+254720284862
Email
wansiste07@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
HELENA DR Coordinating Principal Investigator, PhD
Organizational Affiliation
MEDECIN SAN FRONTIERES
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Diagnostic Performance of a Novel Lipoarabinomannan.
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