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。
研究者
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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