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A Trial of the Urine LAM Strip Test for TB Diagnosis Amongst Hospitalized HIV-infected Patients (LAMRCT)

Primary Purpose

Tuberculosis

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Urine LAM strip test
Sponsored by
University of Cape Town
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Tuberculosis focused on measuring urine LAM strip test, diagnostics, tuberculosis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • HIV-infected (1x rapid HIV test positive)
  • Considered TB suspect by attending doctor (must comprise at least 1 of the following: current fever or cough, drenching night sweats, self-reported LOW)
  • Illness severity sufficient to warrant hospitalization
  • ≥18 years old
  • Provision of informed consent

Exclusion Criteria:

  • HIV-uninfected
  • Patients receiving any anti-TB medication in the 60 days prior to testing
  • Unable to provide 30mls urine
  • Inability to provide informed consent

Sites / Locations

  • University of Cape Town
  • Mbeya Medical Research Programme
  • University Teaching Hospital
  • University of Zimbabwe

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

LAM plus standard care

Standard care

Arm Description

Patients allocated to this study arm will receive urine LAM strip testing in addition to the standard TB diagnostic tools WHO approved and available at each site

Patients allocated to this study arm will receive standard TB diagnostics currently WHO approved and available at the study site

Outcomes

Primary Outcome Measures

All-cause mortality
All-cause mortality at 8-weeks after study enrollment

Secondary Outcome Measures

Change in TB-related morbidity score
Comparative change in TB score between baseline and 8 weeks after enrollment
Change in Karnofsky performance index
Comparative changes in the Karnofsky performance index between baseline and 8 weeks following enrollment
Hospital length of stay
This is the number of days of hospital admission for enrolled patients up to a maximum of 8 weeks post enrollment.
Diagnostic accuracy of urine LAM strip test
Diagnostic accuracy (sensitivity, specificity, predictive values and likelihood ratios) of the urine LAM strip test using TB culture as the diagnostic reference standard

Full Information

First Posted
January 11, 2013
Last Updated
June 1, 2015
Sponsor
University of Cape Town
Collaborators
University of Zimbabwe, University of Zambia, NIMR - Mbeya Medical Research Programme
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1. Study Identification

Unique Protocol Identification Number
NCT01770730
Brief Title
A Trial of the Urine LAM Strip Test for TB Diagnosis Amongst Hospitalized HIV-infected Patients
Acronym
LAMRCT
Official Title
A Randomized Controlled Trial to Evaluate the Impact of Using a Point-of-care Urine LAM Strip Test for TB Diagnosis Amongst Hospitalized HIV-infected Patients in Resource-poor Settings
Study Type
Interventional

2. Study Status

Record Verification Date
June 2015
Overall Recruitment Status
Completed
Study Start Date
January 2013 (undefined)
Primary Completion Date
December 2014 (Actual)
Study Completion Date
January 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Cape Town
Collaborators
University of Zimbabwe, University of Zambia, NIMR - Mbeya Medical Research Programme

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The novel urine LAM point-of-care strip test offers potential clinical utility to improve TB diagnosis in HIV co-infected patients. Urine LAM strip test performance improves with increasing illness severity and more advanced immunosuppression, thus offering the greatest potential utility in hospitalised HIV-infected patients with advanced immunosuppression (CD4 cell count less than 200). However, in the context of high rates of empiric treatment and the availability of other novel TB diagnostics, the clinical impact of the urine LAM strip test is unknown. This study will investigate the impact of the urine LAM strip test. The study hypothesis is that the urine LAM strip test, when combined with standard TB diagnostics (smear microscopy and culture) will significantly improve TB treatment-related outcomes (TB-related mortality, morbidity and length of hospital stay) in HIV-infected hospitalized patients when compared to standard TB diagnostics alone.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tuberculosis
Keywords
urine LAM strip test, diagnostics, tuberculosis

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2618 (Actual)

8. Arms, Groups, and Interventions

Arm Title
LAM plus standard care
Arm Type
Experimental
Arm Description
Patients allocated to this study arm will receive urine LAM strip testing in addition to the standard TB diagnostic tools WHO approved and available at each site
Arm Title
Standard care
Arm Type
No Intervention
Arm Description
Patients allocated to this study arm will receive standard TB diagnostics currently WHO approved and available at the study site
Intervention Type
Device
Intervention Name(s)
Urine LAM strip test
Other Intervention Name(s)
Determine TB urine LAM Antigen strip test
Intervention Description
This is a point-of-care lateral flow strip test to detect the presence of lipoarabinomannan (LAM) in patient urine samples. Only patients with a grade 2-5 visual band intensity will be considered positive and commenced on treatment
Primary Outcome Measure Information:
Title
All-cause mortality
Description
All-cause mortality at 8-weeks after study enrollment
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Change in TB-related morbidity score
Description
Comparative change in TB score between baseline and 8 weeks after enrollment
Time Frame
Baseline and 8 weeks
Title
Change in Karnofsky performance index
Description
Comparative changes in the Karnofsky performance index between baseline and 8 weeks following enrollment
Time Frame
Baseline and 8 week
Title
Hospital length of stay
Description
This is the number of days of hospital admission for enrolled patients up to a maximum of 8 weeks post enrollment.
Time Frame
Date of hospital discharge (max 8 weeks) minus date of admission
Title
Diagnostic accuracy of urine LAM strip test
Description
Diagnostic accuracy (sensitivity, specificity, predictive values and likelihood ratios) of the urine LAM strip test using TB culture as the diagnostic reference standard
Time Frame
8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: HIV-infected (1x rapid HIV test positive) Considered TB suspect by attending doctor (must comprise at least 1 of the following: current fever or cough, drenching night sweats, self-reported LOW) Illness severity sufficient to warrant hospitalization ≥18 years old Provision of informed consent Exclusion Criteria: HIV-uninfected Patients receiving any anti-TB medication in the 60 days prior to testing Unable to provide 30mls urine Inability to provide informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Keertan Dheda, MD
Organizational Affiliation
UCT Lung Infection and Immunity Unit
Official's Role
Study Director
Facility Information:
Facility Name
University of Cape Town
City
Cape Town
State/Province
Western Cape
ZIP/Postal Code
7945
Country
South Africa
Facility Name
Mbeya Medical Research Programme
City
Mbeya
Country
Tanzania
Facility Name
University Teaching Hospital
City
Lusaka
Country
Zambia
Facility Name
University of Zimbabwe
City
Harare
Country
Zimbabwe

12. IPD Sharing Statement

Citations:
PubMed Identifier
22362849
Citation
Peter JG, Theron G, van Zyl-Smit R, Haripersad A, Mottay L, Kraus S, Binder A, Meldau R, Hardy A, Dheda K. Diagnostic accuracy of a urine lipoarabinomannan strip-test for TB detection in HIV-infected hospitalised patients. Eur Respir J. 2012 Nov;40(5):1211-20. doi: 10.1183/09031936.00201711. Epub 2012 Feb 23.
Results Reference
background
PubMed Identifier
22015305
Citation
Lawn SD, Kerkhoff AD, Vogt M, Wood R. Diagnostic accuracy of a low-cost, urine antigen, point-of-care screening assay for HIV-associated pulmonary tuberculosis before antiretroviral therapy: a descriptive study. Lancet Infect Dis. 2012 Mar;12(3):201-9. doi: 10.1016/S1473-3099(11)70251-1. Epub 2011 Oct 17.
Results Reference
background
PubMed Identifier
23099073
Citation
Peter JG, Theron G, Dheda K. Urine antigen test for diagnosis of HIV-associated tuberculosis. Lancet Infect Dis. 2012 Nov;12(11):825; author reply 826-7. doi: 10.1016/S1473-3099(12)70220-7. No abstract available.
Results Reference
background
PubMed Identifier
26970721
Citation
Peter JG, Zijenah LS, Chanda D, Clowes P, Lesosky M, Gina P, Mehta N, Calligaro G, Lombard CJ, Kadzirange G, Bandason T, Chansa A, Liusha N, Mangu C, Mtafya B, Msila H, Rachow A, Hoelscher M, Mwaba P, Theron G, Dheda K. Effect on mortality of point-of-care, urine-based lipoarabinomannan testing to guide tuberculosis treatment initiation in HIV-positive hospital inpatients: a pragmatic, parallel-group, multicountry, open-label, randomised controlled trial. Lancet. 2016 Mar 19;387(10024):1187-97. doi: 10.1016/S0140-6736(15)01092-2. Epub 2016 Mar 10.
Results Reference
derived

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A Trial of the Urine LAM Strip Test for TB Diagnosis Amongst Hospitalized HIV-infected Patients

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