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The Western Galilee Hospital in Nahariya Home Monitoring Registry

Workload Assessment of a Home Monitoring Based Follow up for Biotronik ICD and CRTD Patients.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01548755
Enrollment
20
Registered
2012-03-08
Start date
2012-04-30
Completion date
2015-01-31
Last updated
2012-03-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tachycardia

Keywords

Home monitoring, cardiomessenger, ICD

Brief summary

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

Detailed 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.

Interventions

None listed

Sponsors

ron sela
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Approved indication for ICD or CRTD. * Implanted with or replaced with a Biotronik Lumax device. * Patient is willing and able to sign consent form. * Willing and able to attend clinic visits and follow up schedule. * Transmission of more than 80% at 3-month FU. * Patient older than 18 years.

Exclusion criteria

* No indication for ICD or CRTD implant. * Life expectancy shorter than 12 months. * Pregnancy. * Participation in other clinical studies

Countries

Israel

Contacts

Primary ContactRon Sela, MD
Ron.Sela@naharia.health.gov.il972 4 9107438

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026