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临床试验/NCT03501836
NCT03501836已完成不适用

Performance Evaluation Study of a Six Electrode (8 Lead) Wireless Handheld ECG Recording Device With Four Lead Chest Extension Versus Conventional 12-lead ECG in Heart Patients

Manchester University NHS Foundation Trust1 个研究点 分布在 1 个国家目标入组 271 人开始时间: 2017年1月24日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
271
试验地点
1
主要终点
Capabilities of an 8 lead ECG system (Rapid Rhythm) - normal ECGs

研究概览

简要总结

This study is designed to compare the performance of both 6 and 10 electrode ECGs from the handheld device with the conventional 12 lead ECG. As well as comparing the detection of atrial fibrillation, the study will also compare the detection of other heart problems and of normal heart rhythm.

详细描述

An Electrocardiogram (ECG) 6 electrode, wireless handheld device held on the chest is being developed to allow diagnosis of heart rhythm problems without the need for connecting electrodes to the chest, arms and legs as in a standard 10 electrode (referred to as a 12-lead) ECG measurement. A faster and simpler yet accurate method for acquiring ECG data may be useful in many healthcare settings, including screening for irregular heart rhythms such as Atrial Fibrillation (AF), which is a risk factor for stroke. The wireless 6 electrode device has an extension arm for the handset with 4 additional electrodes (also positioned on the chest) to give a full 12 lead ECG signal. This study is designed to compare the performance of both 6 and 10 electrode ECGs from the handheld device (used on the chest with the subject seated) with the conventional 12 lead ECG (used with electrodes on the chest, arms and legs with the subject lying down). As well as comparing the detection of atrial fibrillation, the study will also compare the detection of other heart problems and of normal heart rhythm. Adult patients attending the clinics at Central Manchester University Hospitals NHS Foundation Trust for an ECG assessment are eligible to participate in the study. A maximum of 500 patients will be recruited to the study in order to find the number of cases with Atrial Fibrillation required to properly compare the methods. A subset of patients with normal ECGs will have additional measurements with both methods whilst lying down, reclining at an angle and sitting upright to investigate any effects of body posture on chest based ECGs.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

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

入选标准

  • •Patient attending an adult cardiology or anti-coagulation clinic appointment, at clinics at Central Manchester University Hospitals NHS Foundation Trust (including the Manchester Heart Centre).
  • •Patients on cardiac wards 3 and
  • •Aged 18 years or above.
  • •Male or Female.

排除标准

  • •Aged less than 18 years.
  • •Unable to give informed consent.
  • •Does not wish to participate in the study.
  • •Any patients with visible breaks to the skin, rashes or inflammation in the chest area on the day of the test
  • •Bedridden or otherwise unable to transfer between chair and bed for both seated and supine measurements

研究组 & 干预措施

Rapid Rhythm Handheld 8-lead ECG Device

Experimental

Participants will have measurements taken with the 8 lead ECG system, which will be compared to the conventional standard care 12 lead ECG.

干预措施: Rapid Rhythm Handheld 8-lead ECG Device (Device)

结局指标

主要结局

Capabilities of an 8 lead ECG system (Rapid Rhythm) - normal ECGs

时间窗: 18 months

The percentage of ECGs where a normal control ECG is matched by a normal RR ECG.

Capabilities of an 8 lead ECG system (Rapid Rhythm) - abnormal ECGs

时间窗: 18 months

The percentage of ECGs where abnormalities of the control ECG are matched by similar abnormalities of the RR ECG.

次要结局

未报告次要终点

研究者

申办方类型
Other Gov
责任方
Sponsor

研究点 (1)

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