跳至主要内容
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 人待定

概览

阶段
4 期
干预措施
未指定
疾病 / 适应症
未指定
发起方
Skanray India
入组人数
28
状态
已完成
最后更新
4年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
待定
结束日期
2017年8月30日
最后更新
4年前
研究类型
Interventional

研究者

发起方
Skanray India

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

结局指标

主要结局

未指定

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