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Sheba Medical Center Home Monitoring Clinic Registry

Sheba Medical Center Home Monitoring Clinic Registry

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01154205
Enrollment
100
Registered
2010-06-30
Start date
2010-06-30
Completion date
2012-01-31
Last updated
2010-06-30

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

Conditions

Clinical Workload Assessment Based Upon a Home Monitoring System

Brief summary

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

Sheba Medical Center
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Approved indication for ICD or CRTD * Implanted with or replaced with a Biotronik Lumax device * Patient 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 follow up * 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 ContactDavid Luria, MD
dluria@sheba.health.gov.il972-52-6667111

Outcome results

None listed

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