CardioSenseSystem Compared Study Regarding Efficacy and Safety in the Monitoring of ECG

Unstable Angina Clinical Trial

Official title:

CardioSenseSystem Compared to Philips Telemetry System Regarding Efficacy and Safety in the Monitoring of ECG

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03610529
• Other study ID #: NovoECG
• Secondary ID: 5.1-2018-1834320
• Status: Not yet recruiting
• Phase: N/A
• Start date: September 2020
• Est. completion date: December 30, 2020

Study information

• Verified date: September 2020
• Source: Novosense AB
• Contact: Jonas Tilly
• Phone: +46709905725
• Email: jonas.tilly[@]novosense.se
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a prospective, controlled, comparative clinical trial of a new ECG monitoring system CardioSenseSystem prior CE marking. The aim of the study is to demonstrate that the CardioSenseSystem's cable-free ECG monitoring system (investigational device) is equivalent or better than traditional and accepted industry standard for cable-based ECG monitoring system (control device). In this study accepted industry standard is Philips Intellivue. In order to investigate this, the study will measure ECG monitoring interruptions, management time and alarm performance. The study population will consist of sixty (60) adult subjects requiring ECG and that are fulfilling the eligibility criteria for study participation. The subjects will be using both the investigational device and the control device simultaneous for measuring data loss, management time and alarm function up to 24 hours.

Description:

A prospective, controlled and comparative clinical trial before CE marking of a new ECG monitoring system CardioSenseSystem. The study population will consist of sixty (60) adult subjects requiring ECG and that are fulfilling the eligibility criteria for study participation. The subjects will be monitored by both the investigational device and the control device for measuring data loss, management time and alarm function up to 24 hours. The duration of the study is estimated to 4 months.

CardioSenseSystem is designed to provide wireless high-quality ECG monitoring. The system developed by Novosense AB consists of three components: the CardioPatch, the Novosense Base Station and the Back-End System. The CardioPatch is a wireless sensor capable to record and transmit ECG data. The CardioPatch send ECG data to the Novosense Base Station, which is the receiving unit. The Back-End System is used for presentation, storage and processing of ECG information. The CardioPatch sensor is applied to the body with an adhesive in the same way as a traditional ECG electrode. In contrast, the CardioPatch is a fully integrated unit containing electrodes, ECG amplifier and a radio transmitter. Novosense's wireless ECG sensors, CardioPatch, transmits the ECG signal 24 hours to the Novosense Base Station receiver.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 60
• Est. completion date: December 30, 2020
• Est. primary completion date: December 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Male or female at least 18 years old.

2. Patient hospitalized at the investigational site and in need of ECG monitoring.

3. Patient with expected alarms during the 24 hours ECG monitoring.

4. Patient who has been informed of the clinical trials purpose, limitations and relevance, and who has voluntarily agreed to participation in the clinical trial by signing the informed consent form.

Exclusion Criteria:

1. Patient with burns.

2. Patient with known allergy or sensitivity to any of the compositions in CardioPatch.

3. Patient with infection in the area where the electrodes are to be placed.

4. Patient with fragile skin (eg after prolonged cortisone treatment).

5. Patient with open sternum / sternum (eg severe heart failure postoperatively) or treatment for infection of the sternum.

6. Patient with mechanical auxiliary heart or ECMO.

7. Patient with implantable defibrillator.

8. Severely ill patient during end of life.

9. Patient participating in any other clinical trial.

10. Patient where the investigator judge that participation may be risky for the patient or obstruct or interfere the implementation of the trial as approved.

Related Conditions & MeSH terms

• Angina, Unstable
• Arrhythmias, Cardiac
• Cardiac Arrythmias
• Disease
• Disorder of Aorta
• Heart Valve Diseases
• Heart Valve Disorders
• Unstable Angina

Intervention

Device:
• CardioSenseSystem
CardioSensySystem is a novel wireless ECG monitoring system developed by Novosense AB for monitoring of ECG in health care departments.
• Philips Intellivue
Philips Intellivue in an established ECG monitoring system used at the clinical investigational device.

Locations

Country	Name	City	State
Sweden	VO Thorax o Kärl, Region Skåne	Lund	Entrégatan 7

Sponsors (1)

Lead Sponsor	Collaborator
Novosense AB

Country where clinical trial is conducted

Sweden, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Lost of monitoring data	Compare time of interruptions in the monitoring system between the investigational device and the control device.	During 24 hour per subject
Secondary	Management time	Compare management time between the investigational device and the control device. This is done by measuring the time required for the sterilization of cables, battery replacements, application of electrodes and cables, and extra management time for applying electrodes and cables if unconnected.	During 24 hour per subject
Secondary	Number of correct yellow and red alarm	Compare the number of correct yellow and red alarm between the investigational device and the control device.	During 24 hour per subject
Secondary	Number of false yellow and red alarm	Compare the number of false yellow and red alarm for the investigational device and the control device.	During 24 hour per subject
Secondary	Incidence and severity of Averse Events	The incidence and severity of adverse events associated with the investigational device and the control device.	During 24 hour per subject

External Links

•   Sponsors website