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临床试验/NCT01693224
NCT01693224Unknown不适用

Feasibility of Using the Inverness Lateral Flow Urine LAM Test for Diagnosis of Tuberculosis in HIV-Positive TB Suspects in Cape Town, South Africa

Tuberculosis Clinical Diagnostics Research Consortium2 个研究点 分布在 1 个国家目标入组 512 人开始时间: 2011年4月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
512
试验地点
2
主要终点
Sensitivity of the lateral-flow urine LAM assay (LF-LAM)

研究概览

简要总结

The purpose of this study is to evaluate the accuracy, diagnostic yield, operational performance, and time to diagnosis of a novel lateral-flow urine LAM test in detecting tuberculosis in HIV-infected adults.

A secondary study objective is to evaluate the accuracy and diagnostic yield of the Cepheid Xpert MTB/Rif test in detecting tuberculosis in the blood of HIV-infected adults.

详细描述

Background: Tuberculosis (TB) incidence and mortality have increased dramatically as a result of the HIV epidemic. In parts of sub-Saharan Africa, TB is the leading cause of death among HIV-infected patients and approximately 50% of TB patients are HIV co-infected. Early treatment of TB is hindered by the lack of rapid, accurate diagnostic modalities that can be applied in resource-constrained settings. Mycobacterial culture is the laboratory standard for diagnosis of active TB, but it is costly, requires access to specialized laboratories, and takes weeks to provide results. Sputum smear microscopy detects less than half of HIV-infected TB cases in many settings. The Global Plan to Stop TB has prioritized the development of simple, accurate, inexpensive tests for TB case detection in HIV-positive individuals.

LAM: As a strategy for rapid TB diagnosis, the detection of Mycobacterium tuberculosis antigens has been explored over several decades. Lipoarabinomannan (LAM), a glycolipid component of the outer cell wall of mycobacteria, is an attractive diagnostic target for several reasons: it is heat-stable; cleared by the kidney; detectable in urine; and as a bacterial product, has the theoretical potential to discriminate active TB from latent TB infection independent of human immune responses. A urine test could facilitate TB diagnosis in patients in whom sputum is uninformative or not obtainable, and lacks the infection-control risks associated with sputum production or blood collection. Urine LAM detection may be amenable to simple, rapid, inexpensive point-of-care platforms.

This is a prospective study to evaluate the accuracy, diagnostic yield, operational performance, and time to diagnosis of a novel lateral-flow urine LAM test in detecting tuberculosis in HIV-infected adults. HIV-positive adults suspected to have TB will be enrolled after providing informed consent. Urine will be obtained for testing using the novel lateral flow urine LAM assay and an existing ELISA-based urine LAM assay. Conventional microbiological tests for TB and chest x-rays will also be performed. These tests will be performed on all participants enrolled (target sample size = 500).

A secondary study objective is to determine the accuracy and diagnostic yield of the Cepheid Xpert MTB/Rif test in detecting tuberculosis in the blood of HIV-infected adults (the same set of participants on whom the LAM testing is done; approximate sample size = 500).

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • (Individuals must meet all of the following inclusion criteria in order to be eligible to participate):
  • Informed consent
  • Suspected active tuberculosis
  • Willingness and ability to comply with study procedures
  • Any one or more of the following:
  • Current cough
  • Fever at any time within the preceding 4 weeks
  • Night sweats at any time within the preceding 4 weeks
  • Weight loss within the preceding 4 weeks
  • HIV-positive based on any one or more of the following:
  • written results of a positive HIV antibody test, and/or
  • written results of a positive HIV viral load, and/or
  • documentation in the medical record of positive HIV status by a treating clinician.

排除标准

  • (Any subjects meeting any of the following exclusion criteria at baseline will be excluded from study participation):
  • Multidrug tuberculosis treatment for greater than two days within the previous 60 days
  • Unwillingness or inability to provide a urine sample
  • Known chronic pulmonary condition, e.g. asthma, chronic obstructive pulmonary disease, emphysema
  • Respiratory distress, defined as respiratory rate of >30 or oxygen saturation <90%
  • Any specific condition that in the judgment of the investigator precludes participation because it could affect a subject's safety.

结局指标

主要结局

Sensitivity of the lateral-flow urine LAM assay (LF-LAM)

时间窗: One year

* Conventional TB tests (mycobacterial blood \& sputum culture) will be the reference standard used to calculate sensitivity of the LF-LAM test * Sensitivity is defined as TP/(TP+FN), or the number of true positives over (the number of true positives + the number of false negatives) * "true positive" = a positive LF-LAM result in a patient also having ≥1 culture positive for M. tuberculosis * "false negative" = a negative LF-LAM result in a patient also having ≥1 culture positive for M. tuberculosis

Failure rate of the lateral-flow urine LAM assay

时间窗: One year

Failure rate expressed as the proportion of lateral flow urine LAM tests that require repeating due to an unevaluable initial result

Inter-reader variability of the lateral-flow urine LAM assay

时间窗: One year

Expressed as the percent agreement

Specificity of the lateral-flow urine LAM assay (LF-LAM)

时间窗: One year

* Conventional TB tests (blood \& sputum culture) will be the reference standard used to calculate specificity (Sp) of the LF-LAM * Sp=TN/(TN+FP), or #true negatives / (#true negatives + #false positives) * "true negative" = negative LF-LAM in "Not TB" patient * "false positive" = positive LF-LAM in "Not TB" patient * "Not TB" = meets all criteria below * no sputum/blood culture positive for MTB * no smear microscopy positive for acid-fast bacilli * no granulomas/caseous necrosis on histopathology * no clinical response to TB treatment * a plausible alternative diagnosis

次要结局

  • Sensitivity of the ELISA-based urine LAM test(One year)
  • Diagnostic yield (expressed as number of TB cases detected) of various diagnostic strategies (see description)(One year)
  • Time to diagnosis (expressed in days) of various diagnostic strategies (see description)(One year)
  • Accuracy, efficiency, costs, and cost-effectiveness of various combinations of TB diagnostic tests(One year)
  • Satisfaction of lateral-flow urine LAM test operators(One year)
  • Specificity (Sp) of the ELISA-based urine LAM test(One year)
  • Sensitivity of the Xpert MTB/Rif test to detect MTB in blood(One year)

研究者

发起方
Tuberculosis Clinical Diagnostics Research Consortium
申办方类型
Network
责任方
Sponsor

研究点 (2)

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