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Clinical Trials/NCT01154205
NCT01154205UnknownNot Applicable

Sheba Medical Center Home Monitoring Clinic Registry

Sheba Medical Center1 site in 1 country100 target enrollmentStarted: June 2010Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
100
Locations
1
Study OverviewStudy DesignEligibility CriteriaInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

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

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts 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

Investigators

Sponsor Class
Other Gov

Study Sites (1)

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