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临床试验/CTRI/2021/03/032094
CTRI/2021/03/032094尚未招募未知

Assessing the accuracy of point-of-care abdominal and thoracic ultrasound for the diagnosis and therapy monitoring in patients with presumed tuberculosis in India and Germany - ALL POCUS

German Infectious Disease Research Center DZIF0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • patients aged 16 years or older
  • -presenting with symptoms compatible with pulmonary TB (PTB) and/or extra-pulmonary (EPTB): At least one of the symptoms below suggestive of TB (as defined by WHO):
  • oCurrent cough of 2 weeks or of any duration in PLHIV
  • oNight sweats
  • oWeight loss
  • -in Germany another group to enrol will be: patients referred to the study sites because TB is presumed due to radiological, histopathological evidence and where a further TB workup is planned (recognizing the selection bias in the analysis plan)
  • -Willingness to have a study follow-up visit at 2-3 months after enrolment (e.g. not planning to relocate). Sonographic follow-up (primary objective 3):
  • -For patients with sonographic findings of TB disease who are treated with anti-TB drugs and who give consent for follow-up ultrasound, US will be repeated at defined timepoints

排除标准

  • -no consent given
  • -already confirmed diagnosis of TB (by sputum microscopy, culture, PCR)
  • -on anti-tuberculous treatment for more than 24 hours
  • -on anti-tuberculous treatment within the past 60 days
  • -on preventive therapy for TB infection within the past 6 months
  • -Patients presenting with presumed peripheral lymph node TB

研究者

发起方
German Infectious Disease Research Center DZIF

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