跳至主要内容
临床试验/NCT01845506
NCT01845506Unknown不适用

The Application of a Wireless Sensor Technology for Vital Statistics in CHILDREN AND ADULTS

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's2 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2021年12月1日最近更新:
适应症

试验速览

阶段
不适用
入组人数
500
试验地点
2
主要终点
Level of agreement between cardiorespiratory monitor and sensor information for temperature

研究概览

简要总结

The primary outcome for this project will be the development of a small, non-invasive wireless sensor that is linked to a conventional computer that can be used in health care for monitoring of acute and chronic health problems. The advantages of developing this technology are threefold. First, monitoring can be conducted for a fraction of the cost of a bedside nurse. Second, monitoring can be done in real time and stored so that we can diagnose and manage critical events in a more timely manner. Lastly, many patients can be monitored simultaneously. The wireless sensors will be fitted to healthy volunteers of various ages. The data gathered from the sensor with respect to their vital signs will be compared to that of conventional tools such as nursing assessments and pulse oximetry.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Adults with controlled and non-controlled hypertension (hypertension defined as > 130/90 on two separate occasions and history of hypertension)
  • Adults with known chronic obstructive pulmonary disease in respiratory distress with oxygen saturations < 90%
  • Febrile adults (temp at triage > 38 C) with no significant co-morbidities
  • Elderly (>70 years) patients with no significant co-morbidities
  • Obese adults (BMI > 30)
  • Febrile (temp at triage > 38 C) and non-febrile children (age < 18 yrs)
  • Obese children (BMI > 30)
  • Neonates (age < 6 weeks)
  • Children with corrected cyanotic congenital heart disease
  • Children in respiratory distress that present with oxygen saturations < 90%

排除标准

  • Subjects with unstable vital signs will be excluded.

结局指标

主要结局

Level of agreement between cardiorespiratory monitor and sensor information for temperature

时间窗: 2 hours

The primary outcome is the level of agreement between conventional methods and sensor information for temperature.

Level of agreement between cardiorespiratory monitor and sensor information for blood pressure

时间窗: 2 hours

The primary outcome is the level of agreement between conventional methods and sensor information for blood pressure.

The primary outcome is the level of agreement between cardiorespiratory monitor and sensor information for heart rate.

时间窗: 2 hours

The primary outcome is the level of agreement between conventional methods and sensor information for heart rate.

Level of agreement between cardiorespiratory monitor and sensor information for oxygen saturation

时间窗: 2 hours

The primary outcome is the level of agreement between conventional methods and sensor information for oxygen saturation.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Naveen Poonai

Assistant Professor

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

研究点 (2)

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