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Clinical Trials/NCT03068169
NCT03068169
Unknown
Not Applicable

Biomedical Shirt-based ECG Monitoring in Relevant Clinical Situations

Medical University of Warsaw3 sites in 1 country220 target enrollmentJune 15, 2017
ConditionsECG Monitoring

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
ECG Monitoring
Sponsor
Medical University of Warsaw
Enrollment
220
Locations
3
Primary Endpoint
Assessment of the impact of the use of a pedometer combined with nECG shirt on the level of daily physical activity and its intensity.
Last Updated
8 years ago

Overview

Brief Summary

Cardiovascular diseases (CVD) are associated with high healthcare costs, as well as are a leading cause of mortality and hospitalizations. The main challenge for today's researchers is to develop new technologies, which may help to improve diagnosis of CVD, thereby reducing healthcare costs and quality of patients' lives. Non-invasive wearable electronics offer new capabilities for the diagnosis and management of patients with CVD. Several reports with wearable electronics have been published, in which achieved very positive results with high accuracy. Aim of our study is to show utility of biomedical shirt-based ECG monitoring of patients with CVD in different clinical situations using Nuubo® ECG (nECG) system.

Detailed Description

The study is an investigator-initiated, multicentre, prospective observational trial. The study will be carried out in 2 tertiary university hospitals on cardiology wards (adult and pediatric). The study will consist of four independent groups of patients whose ECG will be monitored using the biomedical shirt. The study groups will be as follows: patients after pulmonary veins isolation (PVI), cardiac resynchronization therapy (CRT) recipients, patients during cardiac rehabilitation after myocardial infarction, and pediatric patients with supraventricular tachycardia (SVT) before electrophysiology study (EPS). Approval for all study groups was obtained from institutional review board. ECG platform The system consists of biomedical shirt, electronic device and ECG software. The biomedical shirt captures the electrocardiographic signal via the textile electrodes integrated into the garment. The biomedical shirt enable non-invasive reception of a medical-quality ECG signal through adherence of textile electrodes to the skin. The biomedical shirt-ECG monitoring is based on BlendFix® sensor electrode technology that is capable of being used in real-time and for continuous recording. To the shirt is attached the electronic device that transmits the ECG signal (as well as other signals including accelerometer and GPS) via bluetooth to a computer and stores the information in memory cards. The software allows the visualisation and analysis of data such as ECG, heart rate, activity index and relative position of the body captured by the electronic device. The platform is a medical device certified in the European Union that has been tested in patients who underwent an exercise echocardiography test.

Registry
clinicaltrials.gov
Start Date
June 15, 2017
End Date
December 31, 2018
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Medical University of Warsaw
Responsible Party
Principal Investigator
Principal Investigator

Marcin Grabowski

Clinical Professor

Medical University of Warsaw

Eligibility Criteria

Inclusion Criteria

  • PVI in a patient with paroxysmal AF
  • 18 - 70 years old
  • Signed written informed consent Exclusion criteria
  • BMI ≥35 kg/m2
  • Chronic inflammatory disease, severe chronic kidney disease,
  • Active cancer, and a period of 5 years from the end of treatment
  • Use of antiarrhythmic agents after PVI
  • Persistent AF
  • Previous PVI
  • The size of the chest that prevents wearing biomedical shirt

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Assessment of the impact of the use of a pedometer combined with nECG shirt on the level of daily physical activity and its intensity.

Time Frame: 12 month

Association between early recurrences of atrial tachyarrhythmias (ERAT) during blanking period on long-term effectiveness of pulmonary veins isolation (PVI) using nECG shirt.

Time Frame: 13 months

Assessment of the rationale for the use of blanking period and to determine whether the early recurrences of atrial tachyarrhythmias (ERAT) burden influences on long-term effectiveness of pulmonary veins isolation (PVI) using nECG shirt. The study might demonstrate which patients with ERAT remain at risk of long-term recurrence of atrial fibrillation (AF).

Assessment of the usefulness of nECG shirt in detection of fusion and pseudo-fusion beats in cardiac resynchronization therapy (CRT) recipients.

Time Frame: 7 months

Creation of an algorithm based on nECG monitoring using wearable shirt to differentiate atrioventricular reentry tachycardia (AVRT) with atrioventricular nodal reentry tachycardia (AVNRT) in pediatric patients suffering from supraventricular tachycardia.

Time Frame: 1 month

Secondary Outcomes

  • Assessment of the influence of CRT implantation on amount of physical activity measured by nECG shirt.(7 month)

Study Sites (3)

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