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临床试验/NCT01747460
NCT01747460已完成不适用

Controlled Acute Hypoxia Studies Using a Bedside Respiratory Patient Monitoring System With the Functional Patient Monitoring PCBA-1

Medtronic - MITG1 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2012年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
25
试验地点
1
主要终点
SpO2 Accuracy (percentage of blood oxygen saturation)

研究概览

简要总结

To determine accuracy specifications of the Pulse oximeter.

研究设计

研究类型
Observational
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

  • Male or female subjects between the ages of 18 to 50 years (inclusive).
  • Must undergo a physical examination by a licensed physician, advanced practice nurse or physician assistant, including a 12 lead ECG, a medical history, and a blood test checking complete blood count and screening for sickle cell trait or disease
  • All female volunteers must have a negative urine pregnancy test prior to participation.

排除标准

  • Pregnancy or lactating women
  • Unexplained syncopal episodes
  • Hypertension (defined as a systolic pressure of >145 mmHg or a diastolic pressure >90 mm Hg on three consecutive readings)
  • Premature ventricular contractions (PVC's) that are symptomatic or occur at a rate of more than 5/minute
  • History of seizures (except childhood febrile seizures) or epilepsy
  • Routine use of tranquilizers and/or excessive anxiety
  • History of frequent headaches or migraines
  • History of stroke
  • Previous injury or trauma to fingers or hands that may change blood flow or vascular supply and affect our ability to test multiple sensors
  • History of "altitude sickness" defined as headaches, malaise or dizziness when in the mountains or in an aircraft at altitude significantly above sea level for a prolonged period of time (> 1 hour)
  • History of significant respiratory disease, such as severe asthma, emphysema, etc.
  • Sickle cell disease or trait.
  • The use of medications, pre-existing medical conditions, treatment for a medical condition or any other reason deemed relevant by the clinician conducting the study.
  • Abnormal ECG finding
  • Prior or known allergies to lidocaine (or similar pharmacologic agents, e.g., Novocain)
  • Prior or known allergies to heparin.
  • History of transient ischemic attacks or carotid artery disease
  • History of myocardial ischemia, angina, myocardial infarction, congestive heart failure or cardiomyopathy
  • History of chronic renal impairment
  • History of recent arterial cannulation (less than 1 month prior to study)
  • History of complications from previous arterial cannulation
  • Current use of blood thinners

结局指标

主要结局

SpO2 Accuracy (percentage of blood oxygen saturation)

时间窗: Duration of subject visit- approx. 1.5 hours

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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