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临床试验/NCT04552015
NCT04552015终止不适用

Pilot Study for Development of Microneedles for Diagnosis of Latent Tuberculosis Infection

The HIV Netherlands Australia Thailand Research Collaboration2 个研究点 分布在 1 个国家目标入组 4 人开始时间: 2021年4月8日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
4
试验地点
2
主要终点
size of induration at 48 hours post-PPD injection

研究概览

简要总结

This study will evaluate new technique, microneedle, to detect latent tuberculosis (TB) in healthy volunteers

详细描述

The cross-sectional study to investigate the effect of microneedle formulations and lengths of Tuberculin PPD microneedles on the delayed-type hypersensitivity response in healthy volunteers.

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
20 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Sex : Male and Female
  • Age : 20-60 years
  • TB contacts or those at risk of TB e.g. health-care workers
  • HIV-negative healthy individuals

排除标准

  • Presence of an acute infection, as determined by investigators
  • Receiving immunosuppression drugs e.g. steroids
  • Having autoimmune diseases e.g. SLE (Systemic Lupus Erythematous)
  • Being pregnant or breastfeeding

结局指标

主要结局

size of induration at 48 hours post-PPD injection

时间窗: 48 hours

Monitoring the response of delayed-type hypersensitivity on the skin by comparing TST to microneedle tests

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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