跳至主要内容
临床试验/NCT04717024
NCT04717024招募中不适用

The Nanowear Wearable Covid-19 Observational and Analysis Trend

Nanowear Inc.2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2020年9月15日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
Nanowear Inc.
入组人数
100
试验地点
2
主要终点
Hosptialized patient data

研究概览

简要总结

The NanoCOAT study is a multi-center, prospective, non-randomized, feasibility, observational, non-significant risk study. The NanoCOAT study will enroll a minimum of 10 and a maximum of 100 subjects in a potential for a multi-site in order to collect data and analyze physiological and biometric trends due to Covid-19.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subject has provided informed consent
  • Male or female over the age of 18 years
  • The patient is currently hospitalized with a primary diagnosis of Covid-19

排除标准

  • Subject is unwilling or unable to wear the vest during hospitalization.
  • Subjects who are pregnant.
  • Subject is intubated or admitted to ICU
  • Subject has an implantable cardiac device (i.e pacemaker or internal cardioverter defibrillator)

结局指标

主要结局

Hosptialized patient data

时间窗: up to 30 days of monitoring leading to discharge or admission to ICU

The primary study endpoint is adequate collection of hospitalized COVID 19 patient health metric data through the Nanowear WMDRS

次要结局

  • Trends in COVID 19 exacerbation(up to 30 days of monitoring leading to discharge or admission to ICU)

研究者

发起方
Nanowear Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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