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临床试验/NCT03080688
NCT03080688已完成不适用

Prizma Pulse Oximeter Evaluation

G Medical Innovations Ltd.0 个研究点目标入组 12 人开始时间: 2016年4月15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
主要终点
Blood oxygen saturation

研究概览

简要总结

This study is intended to evaluate performance of the new design sufficiently to support performance claims for an FDA 510K submission or ISO technical file. Specifically:

  • SpO2 value range 70% to 100%

  • 10 or more subjects, at least 3 of dark pigmentation

  • At least 200 data points

  • Meeting the following test required by the 2013 FDA Guidance on Pulse Oximeters - Premarket Notification Submissions and by ISO 80601-2-61 on Pulse Oximeters:

  • 2013 FDA Guidance on Pulse Oximeters - Premarket Notification Submissions:

  • 4.1. ACCURACY OF PULSE OXIMETERS

  • 4.1.1 IN VIVO TESTING FOR SPO2 ACCURACY UNDER LABORATORY CONDITIONS

  • ISO 80601-2-61:2011 Annex EE.2 and clause 201.12.1.101.2

  • 201.12.1.101 SpO2 accuracy of pulse oximeter equipment

  • 201.12.1.101.2 Determination of SpO2 accuracy

详细描述

The device under test was the Prizma which is a phone cover biometric device that includes reflectance oximetry. This device is a spot checker that requires the patient to hold their finger on the sensor during the measurement. The subjects were asked not to move during the study. In order to get consistent measurements the fingers were taped to the test device. The tape acted mainly as a reminder, and there were some problems with finger movement. A radial arterial cannula was placed in either the left or right wrist of each subject.

Blood gas analysis to determine oxyhemoglobin saturation was performed on an OSM-3® multi-wavelength oximeter (Hemoximeter, Radiometer, Copenhagen). No subject was anemic (Hemoglobin ≤ 10gm•dl-1). Each subject had control data taken at the beginning of each experiment, with two control blood samples drawn while breathing room air. Hypoxia was induced to different levels of oxyhemoglobin saturation (between 70-100%) by having subjects breathe mixtures of nitrogen, room air, and carbon dioxide. Oxyhemoglobin saturation was reduced to a series of targets and stabilized at the plateau value. Each plateau level of oxyhemoglobin saturation was maintained for at least 30 seconds. Two arterial blood samples were then obtained, approximately 30 seconds apart. A total of 24 samples were obtained per subject. Data were recorded by Bickler-Ye lab and provided for analysis.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

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

入选标准

  • Both male and female subjects
  • Healthy subjects capable of undergoing controlled hypoxemia to the levels outlined in the desaturation profile below.
  • Meeting the demographic requirements listed above.

排除标准

  • Smokers or individuals exposed to high levels of carbon monoxide that result in carboxyhemoglobin levels over 3% as tested by the BYL.
  • Subjects who would be placed under medical risk under the desaturation profile listed below.
  • Significant arrhythmia
  • Age below 21 or over 50
  • Pregnant women

结局指标

主要结局

Blood oxygen saturation

时间窗: 2 days

Comparison of Measurements: Prizma Device versus Gold Standard

次要结局

未报告次要终点

研究者

发起方
G Medical Innovations Ltd.
申办方类型
Industry
责任方
Sponsor

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