跳至主要内容
临床试验/CTRI/2024/03/064735
CTRI/2024/03/064735招募中不适用

Evaluating Diagnostic Performance of SMaRT-PCR – a novel, non-invasive diagnostic workflow for detecting pulmonary tuberculosis in children

Dr Kalpana Sriraman4 个研究点 分布在 1 个国家目标入组 1,200 人开始时间: 2024年4月1日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
1,200
试验地点
4
主要终点
Sensitivity, specificity and positive and negative predictive values of SMaRT-PCR

研究概览

简要总结

Diagnosis of pulmonary tuberculosis (TB) is challenging in children as they often have atypical symptoms, non-specific radiological features, are paucibacillary and do not expectorate sputum. Consequently, most children undergo invasive sampling like gastric aspiration (GA) for obtaining microbiological diagnosis necessary for initiating correct treatment. We have developed an innovative, indigenous, non-invasive diagnostic workflow called SMaRT-PCR, which involves 10 minutes of Sampling with a modified Mask and TB-RNA detection with Reverse Transcriptase-PCR. Pilot study showed that the SMaRT-PCR had a 75% sensitivity and 95% specificity for paediatric TB detection. With further refinement, SMaRT-PCR can now detect TB and drug resistance simultaneously up to one week from sample collection with transport at ambient temperature. The proposed study aims to demonstrate and evaluate the clinical utility of SMaRT-PCR in a large paediatric cohort of TB suspects using a hub-and-spoke model in urban and rural settings. A total of 1200 children presenting with TB symptoms will be recruited and tested using SMaRT-PCR and standard diagnostic methods. The SMaRT-PCR’s diagnostic accuracy will be estimated based on clinical evaluation of confirmed, unconfirmed and unlikely tuberculosis. In the same cohort, we will compare SMaRT-PCR’s diagnostic accuracy with CBNAAT/TrueNAT in reference samples (sputum/GA). Furthermore, we will assess the operational adaptability of SMaRT-PCR for clinical use in diverse settings. If validated, this will be a first-of-its-kind indigenously developed technology that could potentially improve tuberculosis confirmation in multitudes of children in India and globally who rely on clinical diagnosis or undergo invasive testing for treatment.

研究设计

研究类型
Observational

入排标准

年龄范围
1.00 Year(s) 至 14.00 Year(s)(—)
性别
All

入选标准

  • Child with signs and symptom(s) suggestive of TB OR Confirmation of pulmonary TB disease at the time of screening with microbiological confirmation of TB disease.

排除标准

  • Children will be excluded from the study if:.
  • They are too sick to provide a sample for SMaRT-PCR as deemed by the clinician
  • They have been given three or more daily doses of TB treatment before the first study sample is taken.

结局指标

主要结局

Sensitivity, specificity and positive and negative predictive values of SMaRT-PCR

时间窗: 24 months and 48 months

次要结局

  • Concordance of resistance determination by SMaRT-PCR with Whole Genome Sequencing(48 months)
  • Prevalence of confirmed paediatric TB among children with presumptive TB(48 months)
  • Understanding operational challenges associated with implementation of SMaRT-PCR diagnostic workflow for paediatric pulmonary TB diagnosis in diverse geographical and resource settings(48 months)

研究者

发起方
Dr Kalpana Sriraman
申办方类型
Other [Principal Investigator]
责任方
Principal Investigator
主要研究者

Dr Kalpana Sriraman

The Foundation for Medical Research

研究点 (4)

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