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临床试验/NCT03240926
NCT03240926
已完成
不适用

Loop Band Validation Study

Spry Health1 个研究点 分布在 1 个国家目标入组 235 人2017年2月21日
适应症COPD

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
COPD
发起方
Spry Health
入组人数
235
试验地点
1
主要终点
Device Equivalence in clinical outcome measures (heart rate, blood oxygenation, carboxyhemoglobin level, end tidal carbon dioxide, and respiratory rate) measured by Arterial Line.
状态
已完成
最后更新
7年前

概览

简要总结

The main purpose of this study is to assess the accuracy of a non-invasive wearable technology in the form of a wristband.

详细描述

The main purpose of this study is to assess the accuracy of a non-invasive wearable technology in the form of a wristband. This wristband (Loop Band) uses optical sensors and spectrometry to measure and estimate vitals as well as a full blood gas panel; comparable to the standard method of an invasive arterial line and pressure transducer. The investigators aim to show equivalence of clinical physiologic outcome measurements with the Loop Band relative to current methods (i.e. arterial lines, etc.). In addition, this study aims to validate this wearable technology as a potential alternative to invasive measurements, to reduce complications, and improve accuracy in regards to patient monitoring.

注册库
clinicaltrials.gov
开始日期
2017年2月21日
结束日期
2018年1月25日
最后更新
7年前
研究类型
Interventional
研究设计
Single Group
性别
All

研究者

发起方
Spry Health
责任方
Sponsor

入排标准

入选标准

  • Patient has capacity to consent for the study.
  • Anesthetic plan for an arterial line for vital sign monitoring during their surgical procedure.

排除标准

  • Active Atrial Fibrillation
  • Active C-difficile
  • Amputation of the arm at the wrist or above
  • The Investigator and/or Clinical Research Nurse will conduct a visual inspection for attributes that may diminish device accuracy. These include but are not limited to: tattoos over the radial artery, burns or heavy scarring over the radial artery, fragile skin, any skin diseases affecting the wrist or arm, Physician discretion-any condition deemed inappropriate that will preclude use of the device.

结局指标

主要结局

Device Equivalence in clinical outcome measures (heart rate, blood oxygenation, carboxyhemoglobin level, end tidal carbon dioxide, and respiratory rate) measured by Arterial Line.

时间窗: intraoperative

Equivalence in clinical outcome measures (heart rate, blood oxygenation, carboxyhemoglobin level, end tidal carbon dioxide, and respiratory rate etc.) with the Loop Band relative to current methods (i.e. arterial lines, etc.) during a surgical procedure.

次要结局

  • Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability](intraoperative)

研究点 (1)

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