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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
Médecins Sans Frontières, Kenya
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for HIV Primary Infection focused on measuring TUBERCULOSIS IN HIV

Eligibility Criteria

15 Years - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

    First Posted
    July 8, 2021
    Last Updated
    August 30, 2021
    Sponsor
    Médecins Sans Frontières, Kenya
    Collaborators
    Epicentre
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    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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