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临床试验/NCT04587921
NCT04587921Unknown不适用

Feasibility and Impact of Remote Oximetry and Cardiac Frequency Monitoring in Patients Hospitalized and Isolated With Covid-19

University of Sao Paulo General Hospital1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2020年6月22日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
90
试验地点
1
主要终点
Feasibility of the system: Determination of the number of valid versus not valid or missed measurements

研究概览

简要总结

The objective of MoxiCov is to monitor the oximetry of patients admitted to the Covid nursery to provide a more detailed assistance expecting to reduce the amount of hypoxia in these patients.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

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

入选标准

  • •Over 18 years old
  • •COVID 19 positive or suspected COVID19

排除标准

  • 未提供

研究组 & 干预措施

Patients monitored with oximeter

Experimental

The first 45 patients will be monitored but the results will not be displayed. The second half of the patients the oximeter will have their monitoring data available online in the ward.

干预措施: Digital oximeter monitoring (Device)

结局指标

主要结局

Feasibility of the system: Determination of the number of valid versus not valid or missed measurements

时间窗: 6 months

Determination of the number of valid versus not valid or missed measurements of each participant.

Hypoxic burden

时间窗: 6 months

Time spent with SpO2\< 93%, 90% and 85%

Satisfaction of the nursing, medical team and patients with the implemented system

时间窗: 6 months

Measurement of NET PROMOTING SCORE (NPS). This score will show the satisfaction of the healthcare team with the device. This score have a minimum of 0 points and maximum of 32 points.

Hypoxic alarm

时间窗: 6 months

Number of times the oximeter record 3 consecutive measurements of SpO2\<90%

次要结局

  • Number of false alarms caused by malfunctions or bad oximeter positioning(6 months)
  • Time of SpO2<90%, SpO2<85% and SpO2<80%(6 months)
  • Total hospital stay(6 months)
  • Time of supplementary oxygen use(6 months)
  • Mortality of participants(6 months)

研究者

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

Geraldo Lorenzi Filho

Associate Professor/PI

University of Sao Paulo General Hospital

研究点 (1)

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