Meir Medical Center Home Monitoring Clinic Registry

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01516112

Enrollment

Registered

2012-01-24

Start date

2012-02-29

Completion date

Unknown

Last updated

2012-01-24

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

Conditions

Patients Implanted With an ICD or CRTD.

Keywords

ICD, home monitoring, cardiomessenger, implant

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

Study design

Observational model

CASE_ONLY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

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 ContactIsrael Chetboun, M.D

shetboun.israel@clalit.org.il+972-577482449

Outcome results