Meir Medical Center Home Monitoring Clinic Registry

• Conditions: Patients Implanted With an ICD or CRTD.

• Registration Number: NCT01516112
• Lead Sponsor: Meir Hospital, Kfar Saba, Israel

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Status Verified: 2011-07
• Study First Submitted: 2012-01-19
• Study First Submitted QC: 2012-01-19
• Last Update Submitted: 2012-01-19
• Study First Posted: 2012-01-24
• Last Update Posted: 2012-01-24
• Study Start: 2012-02

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 20

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

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Trial Locations

Locations (1)

Meir MC; 🇮🇱 Kefar Saba, Israel