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临床试验/CTRI/2021/10/037193
CTRI/2021/10/037193已完成4 期

Pulse Oximetry(SpO2) Device OXYSKANs Accuracy Study as Compared to standard Device: Controlled Desaturation study of OXYSKAN - OXYSKA

Skanray India0 个研究点目标入组 28 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
28

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1)Non-smokers
  • 2)Healthy; no known blood disorders
  • 3)Finger sizes within the sensor specifications
  • 4)Minimum 18 years of age
  • 5)Hb > 10 g/dl

排除标准

  • 1)Artificial nails or fingernail polish
  • 2)Subjects who would be placed at undue medical RISK associated with any PROCEDURES called for in the protocol; a previous or current diagnosis of anemia, asthma, heart/circulatory disease, high blood pressure, emphysema, or an epilepsy or seizure disorder
  • 3)Being diagnosed with pneumonia during the previous year
  • 4)Being a habitual tobacco smoker
  • 5)Having lived at altitudes above 5,000 ft three months prior to being enrolled
  • 6)History of having Claustrophobia
  • 7)Pregnant Female
  • 8)History of alcohol intake in last 48 hours

研究者

发起方
Skanray India

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