跳至主要内容
临床试验/CTRI/2025/08/092157
CTRI/2025/08/092157尚未招募2 期

Rapid Research in Diagnostics Development for TB Network (R2D2 TB Network) Study

National Institutes of Health1 个研究点 分布在 1 个国家目标入组 8,200 人开始时间: 2026年8月17日最近更新:

试验速览

阶段
2 期
状态
尚未招募
入组人数
8,200
试验地点
1
主要终点
This is expected to improve the participants overall TB care and diagnostics.

研究概览

简要总结

The Rapid Research in Diagnostics Development for TB Network (R2D2 TB Network) study seeks to identify and rigorously assess promising early stage tuberculosis (TB) triage and diagnostic tests (hereafter referred to as “novel diagnostics”) in clinical studies conducted in settings of intended use. Rapid diagnosis and effective treatment are critical for improving patient outcomes and reducing TB transmission. However, analysis of care cascades and prevalence surveys indicate that 40-60% of patients with TB are not initiated on effective treatment.1, 2 The different types of tests required to reduce this “diagnostic gap” have been described in the form of target product profiles (TPPs). The highest- priority TPPs are for: 1) a point-of-care, non-sputum biomarker-based test to facilitate rapid TB diagnosis using easily accessible samples (a biomarker test) and 2) a simple, low-cost test that can be used by front-line health workers to rule-out TB (a triage test). The R2D2 TB Network study is a phased evaluation of promising novel TB diagnostics, with iterative assessment of early/late prototypes nested within large-scale validation of design-locked products. In all phases, the accuracy of novel diagnostics will be compared against a reference standard including sputum/urine Gene Xpert® MTB/RIF Ultra and sputum mycobacterial culture, which are standard of care for tests used routinely in patient care.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
12.00 Year(s) 至 90.00 Year(s)(—)
性别
All

入选标准

  • We will include adults and adolescents who are positive for TB and RIF resistance according to routine diagnostic testing (based typically on Xpert MTB/RIF, Xpert MTB/RIF Ultra, or Hain MTBDRplus).

排除标准

  • We will exclude people whohave negative or contaminated results on all baseline (i.e., enrollment) sputum cultures, are unable to provide at least two sputum specimens of 3 mL each or a high-quality specimen with a volume of at least 6 are unable or unwilling to provide informed consent.

结局指标

主要结局

This is expected to improve the participants overall TB care and diagnostics.

时间窗: Cross-sectional study, at TB screening level, which will be the baseline (0 weeks) and Follow-up (2 to 7 monhts)

次要结局

  • To evaluate new tests to diagnose TB more easily & rapidly & rapid diagnosis.(TB screening level (0 weeks), which will be the baseline visit & at follow-up visit (2 to 7 months))

研究者

申办方类型
Government funding agency
责任方
Principal Investigator
主要研究者

Balamugesh Thangakunam

Christian Medical College Vellore

研究点 (1)

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