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Clinical Trials/NCT01516112
NCT01516112UnknownNot Applicable

Meir Medical Center Home Monitoring Clinic Registry

Meir Hospital, Kfar Saba, Israel1 site in 1 country20 target enrollmentStarted: February 2012Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
20
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
Meir Hospital, Kfar Saba, Israel
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

chetboun israel

Dr. Israel Chetboun

Meir Hospital, Kfar Saba, Israel

Study Sites (1)

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