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Clinical Trial Summary

The purpose of this study is to study workload assessment of home monitoring based follow up for ICD or CRTD implanted patient.


Clinical Trial Description

EP unit device clinic is a very busy clinic. Every 6 month the patients arrive for device follow up where the device parameters, patient condition and arrhythmic events are being reviewed, and reprogramming of the device (if needed) is done. Average net time of patient's stay in the clinic is between 30-45 minutes.

Patients implanted with the Lumax device family allows for a better automated follow up procedure via remote management (Home Monitoring).

The purpose of the registry is to assess workload of a Home Monitoring based follow up for Biotronik ICD and CRTD patients. ;


Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT01548755
Study type Observational
Source Western Galilee Hospital-Nahariya
Contact Ron Sela, MD
Phone 972 4 9107438
Email Ron.Sela@naharia.health.gov.il
Status Not yet recruiting
Phase N/A
Start date April 2012
Completion date January 2015

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