Pulse Oximetry Performance Test for PaMo - Controlled Desaturation Test
研究概览
详细说明
The study involves controlled desaturation for voluntary participants, gradually lowering blood oxygen levels by reducing the inhaled air's oxygen content. This reduction is facilitated by the Hypoxico device, simulating high-altitude conditions. The device, connected to a transparent tent placed over subject's upper body, gradually decreases the surrounding air's oxygen content. Oxygen saturation is lowered to a minimum of 70%, and the measurement period lasts a maximum of 30 minutes. A physician and two research team members will be present throughout the measurement. Vital signs, including respiratory rate, heart's electrical activity, blood pressure, and oxygen saturation, will be monitored using the patient monitor in addition to the device being studied. Carbon dioxide levels in exhaled breath will be measured using nasal cannulas.
Reference devices:
Masimo RAD-97 pulse oximeter is a class IIB device and leading technology in measuring SpO2 and has demonstrated high sensitivity and accuracy even during conditions of motion and low perfusion. SpO2 and pulse will be monitored during the measurement period.
GE Carescape B450 is a class IIB device and globally used patient monitor with highly sophisticated algorithms for arrhythmia, non-invasive blood pressure and SpO2. 5-digit ECG, non-invasive blood pressure, IP, SpO2 and pulse will be monitored during the measurement period.
The study does not include a control group. All subjects are using the devices in similar way and the parameters collected from the same individual using two different methods are compared.
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
-
-
-
Tampere、芬兰
- Tampere University
-
-
参与标准
资格标准
适合学习的年龄
- 成人
接受健康志愿者
描述
Inclusion Criteria:
- Age: minimum of 18 years and max 40 years
- ASA category 1
- positive Allen's test
- Passing the physical examination
- Ability to give informed consent
- Volunteering to the study
Exclusion Criteria:
- Age under 18 or over 40 years
- Smoker
- Pregnancy
- Does not pass the physical examination
- Negative Allen's test
- Relevant medical illnesses
- Cardiovascular disease
- Pulmonary disease
- Insufficient knowledge in Finnish or English
- Cardiac pacemaker
- Inability to give informed consent
- Denial
学习计划
研究是如何设计的?
设计细节
- 主要用途:设备可行性
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Controlled desaturation for healthy volunteers
|
Controlled hypoxia induced with Hypoxico device
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Blood Oxygen Saturation Accuracy
大体时间:Continuous measurement up to 30 minutes
|
Average root mean square (ARMS) difference compared with reference device
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Continuous measurement up to 30 minutes
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Hypoxia Detection
大体时间:Continuous measurement up to 30 minutes
|
SpO2 ≤92%
|
Continuous measurement up to 30 minutes
|
合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- PamoSpO2
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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