Non-invasive Mapping of Rhythm Disorders

Status: Completed
Location: See location...
Intervention Type: Device, Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This current care protocol follows the biomedical research protocol entitled Non-invasive mapping of the heart ECG high amplification that demonstrated the clinical value of noninvasive Cardioinsight® mapping system. Guide the management of patients hospitalized for cardiac rhythm radiofrequency ablation of cardiac arrhythmias, implantation or programming of a pacemaker, or assess the risk of serious arrhythmias or sudden death, with the currently used non-invasive mapping routine. The results obtained with non-invasive mapping will be compared with those obtained with the conventional method without non-invasive mapping.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 15
Healthy Volunteers: No
View:

• Oral agreement of the patient or of the holder of parental responsibility after reading the informed consent form.

• Patients with the following 3 conditions :

• Ablation of drugs rebels arrhythmias.

• Or implantation or programming of a pacemaker (pacemaker or defibrillator)

• Or symptoms and / or cardiopathy with risk of sudden death.

Locations
Other Locations
France
CHU de Bordeaux
Bordeaux
Time Frame
Start Date: May 19, 2015
Completion Date: May 28, 2020
Participants
Target number of participants: 492
Treatments
Experimental: Group 1 : Cardiac rythm radiofrequency ablation
Prospective recruitment
Experimental: Group 1: Implantation or programming of a pacemaker
Prospective recruitment
Experimental: Group 1: Risk of serious arrhythmias or sudden death
Prospective recruitment
Active Comparator: Group 2: Cardiac rythm radiofrequency ablation
Retrospective recruitment
Active Comparator: Group 2 : Implantation or programming of a pacemaker
Retrospective recruitment
Active Comparator: Group 2 : Risk of serious arrhythmias or sudden death
Retrospective recruitment
Sponsors
Leads: University Hospital, Bordeaux

This content was sourced from clinicaltrials.gov

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