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临床试验/NCT06633861
NCT06633861
已完成
不适用

Data Collection Study for RFP (Respiration From Plethysmogram)

Philips Clinical & Medical Affairs Global1 个研究点 分布在 1 个国家目标入组 86 人2024年9月5日

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
In-patients Assessment of Vital Signs
发起方
Philips Clinical & Medical Affairs Global
入组人数
86
试验地点
1
主要终点
Data collection for database for algorithm development
状态
已完成
最后更新
7个月前

概览

简要总结

The study will be conducted in hospitalised patients who undergo spot-check monitoring of vital signs as part of their routine care.

详细描述

In an additional spot-check measurement procedure, the study will measure oxygen saturations through different Philips SpO2 finger sensors. Patients will wear a nasal cannula linked to a CO2 measuring device at the same time. The data from both devices will be used to design and improve algorithms for measurement of respiratory rate with the saturation probe and the Philips FAST pulse oximeter system. The study will include 50 adult patients and 25 pediatric patients.

注册库
clinicaltrials.gov
开始日期
2024年9月5日
结束日期
2024年11月7日
最后更新
7个月前
研究类型
Interventional
研究设计
Single Group
性别
All

研究者

入排标准

入选标准

  • Adult subjects (aged 18 years or older) willing and able to understand and provide written informed consent
  • Paediatric subjects aged 16 years and older willing and able to understand and provide written informed consent
  • Paediatric subjects aged approx. 4-16 years and their legal guardians, willing and able to understand and provide written informed consent/assent
  • Subject weight within intended use of at least one SpO2 sensor under test at time of enrolment (M1191T: adult patients \>50kg, M1196T: adult patients \>40kg, M1192A: paediatric patients 15-50kg)
  • Willing and able to wear study devices during study procedures
  • Subject undergoing regular spot-check measurements as per the site's standard of care

排除标准

  • Palliative patients
  • Critically ill patients with severe physiological instability (NEWS ≥9)
  • Injury/wounds or physical malformation of sensor application site (i.e. fingers, toes, hands, feet)
  • Subjects with severe contact allergies to standard adhesives, latex or other materials found in pulse oximetry sensors (self-reported)
  • Unwillingness or inability to remove coloured nail polish or artificial nails from application site
  • Nail fungus on application site
  • Severe dermatitis or hyperkeratosis (e.g. ichthyosis) at sensor application site

结局指标

主要结局

Data collection for database for algorithm development

时间窗: 6 months

Anonymized database of subject data from the Oxygen Saturation finger sensors (photoplethysmogram waveform) and the reference sensors (capnography waveform)

研究点 (1)

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