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CompletedNCT04583904PROVE-TBUpdated Aug 7, 2024

Prospective Evaluation of Novel Diagnostics for Tuberculosis in KwaZulu-Natal, South Africa

An observational study in Tuberculosis, sponsored by University of Washington. Completed at 1 site in South Africa. Open to participants aged 12 Months and older. Per ClinicalTrials.gov, last updated 2024-08-07.

Sponsored by University of Washington · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
843
Ages
12 Months and older
Sex
All
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Study summary

Tuberculosis (TB) infects nearly two billion people and has become the leading infectious cause of mortality worldwide, due in part to inadequate diagnostic and prognostic tests. Older diagnostic tools, such as acid-fast staining, and newer diagnostic tests, such as nucleic acid amplification, are either insensitive, expensive, or not suitable for use at the clinical point-of-care. Therefore, novel diagnostic tests are needed to diagnose active TB disease among adults, people living with HIV (PLHIV), and children in TB-endemic countries. In this project, the investigators will conduct clinical evaluation studies of emerging TB diagnostic tests among (1) hospitalized adults, (2) ambulatory adults in outpatient clinics, and (3) children \<12 years suspected of having active TB disease. the investigators will also maintain a biorepository of well-characterized clinical specimens that can be used for either retrospective validation of TB diagnostic tests, establishing a reference LAM test, or to share with partners developing novel TB diagnostics, including new LAM antibodies. The project will be coordinated at the University of Washington, and conducted in partnership with clinical research partners in South Africa, including Umkhuseli Innovation and Research Management (UIRM) and the National Health Laboratory Service (NHLS). The project team is well-equipped to serve as a central clinical research site to evaluate new and emerging point-of-care TB diagnostics, particularly novel urinary LAM assays, at the on-site TB Diagnostics Research Laboratory at Edendale Hospital in KwaZulu-Natal, South Africa.

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Conditions studied

  • Tuberculosis

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Keywords

  • Urine-Lam
  • Diagnostics
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In context

Tuberculosis

1,417 studies on the registry are indexed under Tuberculosis; 208 are open to participants now.

This study's enrollment of 843 is above the median of 250 across 421 observational studies indexed under Tuberculosis.

Browse Tuberculosis studies →

Lead sponsor

University of Washington is the lead sponsor of 1,397 studies on the registry; 225 are open to participants now.

Of its 154 completed or terminated interventional studies of FDA-regulated products, 132 (86%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
12 Months and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study may enroll 3 different types of patient cohorts, including (1) hospitalized adults (≥16 years old), (2) ambulatory adults (≥16 years old) in outpatient clinics, and (3) children \<12 years suspected of having active TB disease.

Eligibility criteria

Phase I

  1. Eligibility for hospitalized and ambulatory adults:
  • ≥16 years old
  • Positive Xpert MTB/RIF Ultra test (TB-positive cohort) or no suspicion of clinical TB (TB-negative cohort)
  • Have a documented HIV test result or agrees to test for HIV
  • Have NOT received IPT within prior 3 months
  • Have NOT received anti-TB treatment for more than 24 hours
  • Willing/able to provide written informed consent

Phase II:

  1. Eligibility for hospitalized adults:

    • ≥16 years old
    • Admitted to inpatient medical ward \<72 hours
    • Have a documented positive HIV test
    • Have NOT received IPT within prior 3 months
    • Have NOT received anti-TB treatment for more than 24 hours
    • Willing/able to provide written informed consent

    Study population description:

  2. Eligibility for Xpert+ adults (hospitalized and attending outpatient clinics)

    • ≥16 years old
    • Have a documented HIV test result or agrees to test for HIV
    • Positive Xpert MDR/RIF Ultra test documented.
    • Have NOT received anti-TB treatment for more than 24 hours
    • Willing/able to provide written informed consent

      1. Eligibility for children
    • children \<12 years of age
    • suspected of having active TB disease by clinical team
    • Have a documented HIV test result or agrees to test for HIV
    • Have not had IPT within 3 months
    • Have not received anti-TB treatment for more than 24 hours within the prior 5 days
    • Parent or guardian is willing/able to provide written informed consent
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
843 participants (actual)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Adults - inpatient
  • Adults- ambulatory
  • Children
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What researchers measure

Primary outcomes

  1. Number of Participants Classified with TB Case Definition

    TB positive: A person with a positive Xpert MTB/RIF test or TB culture on any bodily fluid specimen that was obtained/tested within 5 days of enrollment. Probable TB: A person with compatible symptoms, signs, histopathological specimens and imaging for TB, but without a positive TB culture or Xpert test on any specimen; empirically initiated on TB treatment. TB negative: A person with a primary hospital diagnosis other than TB, who has no clinical suspicion for TB, and no diagnostic TB testing ordered by the treating team. TB negative (TB excluded): A person with all reference microbiological testing for TB returning negative, including negative Xpert, negative TB culture, other investigations for TB negative (e.g. histopathology, imaging) and either clinical improvement in the absence of anti-TB therapy or alternate diagnosis determined. In addition, no incident TB diagnosis made (including empiric anti-TB treatment initiation) within the 2 months following enrollment.

    Time frame: Baseline

Secondary outcomes

  1. Number of Participants with TB Treatment Outcome

    * Confirmed TB: Bacteriological confirmation obtained: culture or Xpert MTB/RIF from at least one specimen. * Probable TB: Bacteriological confirmation not obtained AND at least 2 of the following: * Symptoms/signs suggestive of TB (as defined) * Chest radiograph or abdominal ultrasound consistent with TB * Close TB exposure or immunologic evidence of M. tuberculosis infection * Positive response to anti-TB treatment (requires documented positive clinical response on TB treatment) * TB negative/unlikely: Bacteriological confirmation NOT obtained AND criteria for "unconfirmed tuberculosis" NOT met.

    Time frame: 2 Month, 6 Month

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Study locations

1 site
  • Edendale Hospital
    Pietermaritzburg, 3201, South Africa
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 7, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04583904
Lead sponsor
University of Washington
Collaborators
Umkhuseli Innovation and Research Management (UIRM), University of KwaZulu, PATH, KwaZulu Natal Department of Health, Salus Ltd.
Responsible party
Paul Drain (Associate Professor of Global Health, Medicine and Epidemiology, University of Washington) — Principal investigator
First posted
Oct 12, 2020
Start date
Sep 18, 2019
Primary completion
Aug 31, 2022
Completion
Aug 31, 2022
Last update
Aug 7, 2024

Study contacts

Paul K. Drain, MD, MPH, FACP
principal investigator · University of Washington
Douglas Wilson, MD
principal investigator · University of KwaZulu

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2024. You cannot join it, but the record below documents what was studied.

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