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Wireless Handheld 8-lead ECG Device Performance in Heart Patients (Rapid Rhythm)

Primary Purpose

Atrial Fibrillation, Heart Murmurs

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Rapid Rhythm Handheld 8-lead ECG Device
Sponsored by
Manchester University NHS Foundation Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Atrial Fibrillation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. 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).
  2. Patients on cardiac wards 3 and 4.
  3. Aged 18 years or above.
  4. Male or Female.

Exclusion Criteria:

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

Sites / Locations

  • Manchester University NHS Foundation Trust

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Rapid Rhythm Handheld 8-lead ECG Device

Arm Description

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

Outcomes

Primary Outcome Measures

Capabilities of an 8 lead ECG system (Rapid Rhythm) - normal ECGs
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
The percentage of ECGs where abnormalities of the control ECG are matched by similar abnormalities of the RR ECG.

Secondary Outcome Measures

Full Information

First Posted
April 9, 2018
Last Updated
September 10, 2019
Sponsor
Manchester University NHS Foundation Trust
Collaborators
Rapid Rhythm Ltd
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1. Study Identification

Unique Protocol Identification Number
NCT03501836
Brief Title
Wireless Handheld 8-lead ECG Device Performance in Heart Patients (Rapid Rhythm)
Official Title
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
Study Type
Interventional

2. Study Status

Record Verification Date
September 2019
Overall Recruitment Status
Completed
Study Start Date
January 24, 2017 (Actual)
Primary Completion Date
June 30, 2019 (Actual)
Study Completion Date
June 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Manchester University NHS Foundation Trust
Collaborators
Rapid Rhythm Ltd

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Fibrillation, Heart Murmurs

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
271 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Rapid Rhythm Handheld 8-lead ECG Device
Arm Type
Experimental
Arm Description
Participants will have measurements taken with the 8 lead ECG system, which will be compared to the conventional standard care 12 lead ECG.
Intervention Type
Device
Intervention Name(s)
Rapid Rhythm Handheld 8-lead ECG Device
Intervention Description
We want to explore whether using 6 electrodes on the chest (as in the Rapid Rhythm Handheld 8-lead ECG device) can give the same diagnostic result to the standard 10 electrode (12-lead) ECG, which uses 6 chest electrodes plus 4 electrodes on the arms and legs. To do this we need to compare measurements taken with the 6 electrode (8 lead) study device to those taken with the gold-standard 10 electrode (12 lead) method. We want to find out whether the new equipment can detect the same heart rhythms as the standard method, so that ECG measurements might be made more quickly and easily in the future.
Primary Outcome Measure Information:
Title
Capabilities of an 8 lead ECG system (Rapid Rhythm) - normal ECGs
Description
The percentage of ECGs where a normal control ECG is matched by a normal RR ECG.
Time Frame
18 months
Title
Capabilities of an 8 lead ECG system (Rapid Rhythm) - abnormal ECGs
Description
The percentage of ECGs where abnormalities of the control ECG are matched by similar abnormalities of the RR ECG.
Time Frame
18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 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 4. Aged 18 years or above. Male or Female. Exclusion Criteria: 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
Facility Information:
Facility Name
Manchester University NHS Foundation Trust
City
Manchester
ZIP/Postal Code
M13 9WL
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No

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Wireless Handheld 8-lead ECG Device Performance in Heart Patients (Rapid Rhythm)

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