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临床试验/NCT06353490
NCT06353490进行中(未招募)不适用

The Clinical Performance Validation of Electronic Thermometer and Infrared Thermometers

Geon Corporation2 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2022年8月12日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
150
试验地点
2
主要终点
Limits of Agreement

研究概览

简要总结

Geon Corporation develops ear thermometers and forehead thermometers that use infrared measurement technology to measure human body temperature. This study verify the accuracy and repeatability of investigational devices. Efficacy verification is carried out by comparing with the referent medical devices.

The main objectives of this study are:

  1. To verify that the investigational devices and the reference medical devices have a reasonable deviation value.
  2. To verify the consistency of repeated measurements of investigational devices.

详细描述

This Study carried out in accordance with the ISO 80601-2-56: 2017, which included definitions for the age groups and sample sizes, the definition of fever, the flowchart for relevant procedures, and statistical methods for clinical performance.

All subjects were measured by the reference device (electronic thermometer MT-B231) and three investigational devices under test evaluation (infrared forehead thermometer GE-TF03, infrared ear thermometer GE-TE06, and electronic thermometer MT-B321FB). For each subject, the reference device measured one time and each investigational device measured three times respectively.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
— 至 80 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Newborn to 80 years old adult
  • Male or Female
  • The subject or parent/guardian can talk to the researcher, understand the content of the study after researcher's explanation and agree to sign the subject's consent form, and is willing to accept the trial procedure.

排除标准

  • Currently have signs or symptoms of infection or inflammation at the temperature measurement site (axillary, forehead, ear canal)
  • The forehead cannot be fully exposed to the environment for more than 15 minutes
  • Using cooling blankets, fans, or placing ice cubes on the forehead
  • There is a catheter placed in the ear
  • Use of antipyretics (such as aspirin, ibuprofen), barbiturates, antipsychotics in the past 2 hours
  • Received thyroxine, corticosteroids or immunotherapy in the past 7 days
  • Subject has been diagnosed with cognitive impairment or has a history of dementia, mental illness, mental illness, pervasive developmental disorder, illicit drug use or alcoholism, etc.
  • Pregnant women
  • The researcher considers that the subject is not suitable for participating in this trial, such as taking any drugs that may change body temperature
  • Participated in clinical trials of investigational drugs within the last 30 days
  • The subject is unwilling to sign the subject's consent form

结局指标

主要结局

Limits of Agreement

时间窗: Through study completion, an average of 2 years

The magnitude of a potential disagreement between investigational thermometer and reference thermometer.

Clinical Bias

时间窗: Through study completion, an average of 2 years

Mean Difference between investigational thermometer and reference thermometer.

Clinical Repeatability

时间窗: Through study completion, an average of 2 years

Pooled standard deviation of triplicate measurements over the entire population of subject

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 (2)

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