跳至主要内容
临床试验/CTRI/2017/11/010590
CTRI/2017/11/010590招募中不适用

Mobile Dengue Diagnostic Technology (m-DDT):A smartphone-based point-of-care diagnostics and early warning system for epidemic prediction, preparedness and control.

Sri Sathya Sai Institute of Higher Learning1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2017年7月18日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
200
试验地点
1
主要终点
Hand-held device for diagnosis, prognosis and differentiation of vector-borne disease, dengue.

研究概览

简要总结

In this work, we intend to develop a portable, hand-heldmedical diagnostic device that will be capable of diagnosis and prognosis ofthe vector-borne disease dengue with genotypic specificity. On realizing theinitial prototype we intend to extend the device’s capability as amulti-analyte sensing platform to evaluate the presence of alternatevector-borne diseases such as: Malaria, Zika and Chikungunya. The novelty ofthis device is the determination of major vector-borne disease infection statusin real time without the need for any high-end equipment or laboratoryprocedures.

研究设计

研究类型
Observational

入排标准

年龄范围
6.00 Year(s) 至 80.00 Year(s)(—)
性别
All

入选标准

  • Age: 6 years to 80 years Disease State: The patient is diagnosed with Dengue if he/she comes in with fever combined with 2 of the following additional symptoms: Headache, Retro-orbital pain, Myalgia, arthralgia, Rash, hemorrhagic manifestations, Petechiae, Purpurae, Platelets <1,00,000, Joint Pains, Hematocrit count >20% from Baseline.

排除标准

  • Patients with previous (past 3 months) blood transfusion and/or platelet transfusion are excluded from the study.
  • Patients below the age of 6 years and pregnant woman are excluded.

结局指标

主要结局

Hand-held device for diagnosis, prognosis and differentiation of vector-borne disease, dengue.

时间窗: First sample is collected at Febrile stage. Second sample is collected at Critical phase. Third sample is collected at recovery phase.

We intend to extend the device’s capability as a multi-analyte sensing platform to evaluate the presence of alternate vector-borne diseases.

时间窗: First sample is collected at Febrile stage. Second sample is collected at Critical phase. Third sample is collected at recovery phase.

次要结局

  • We intend to extend the device’s capability as a multi-analyte sensing platform to evaluate the presence of alternate vector-borne diseases.(4 years)

研究者

申办方类型
Other [Private Academic Institution (Deemed to be University)]

研究点 (1)

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