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临床试验/NCT03710980
NCT03710980已完成不适用

Accuracy of Pulse Oximeters With Profound Hypoxia

Hancock Medical, Inc.1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2018年9月18日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
12
试验地点
1
主要终点
SpO2 Accuracy

研究概览

简要总结

This study to assess the oxygen saturation accuracy of the Beddr SleepTuner in profound hypoxia.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • The subject is male or female, aged ≥18 and <
  • The subject is in good general health with no evidence of any medical problems.
  • The subject is fluent in both written and spoken English.
  • The subject has provided informed consent and is willing to comply with the study procedures.

排除标准

  • The subject is obese (BMI>30).
  • The subject has a known history of heart disease, lung disease, kidney or liver disease.
  • Diagnosis of asthma, sleep apnea, or use of CPAP.
  • Subject has diabetes.
  • Subject has a clotting disorder.
  • The subject a hemoglobinopathy or history of anemia, per subject report or the first bloodsample, that in the opinion of the investigator, would make them unsuitable for study participation.
  • The subject has any other serious systemic illness.
  • The subject is a current smoker.
  • Any injury, deformity, or abnormality at the sensor sites that in the opinion of the investigators' would interfere with the sensors working correctly.
  • The subject has a history of fainting or vasovagal response.
  • The subject has a history of sensitivity to local anesthesia.
  • The subject has a diagnosis of Raynaud's disease.
  • The subject has unacceptable collateral circulation based on exam by the investigator (Allen's test).
  • The subject is pregnant, lactating or trying to get pregnant.
  • The subject is unable or unwilling to provide informed consent, or is unable or unwilling to comply with study procedures.
  • The subject has any other condition, which in the opinion of the investigators' would make them unsuitable for the study.

结局指标

主要结局

SpO2 Accuracy

时间窗: 60 minutes

Collect and analyze data to determine SpO2 accuracy of oximeters under test.

次要结局

未报告次要终点

研究者

发起方
Hancock Medical, Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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