Sheba Medical Center Home Monitoring Clinic Registry

• Conditions: Clinical Workload Assessment Based Upon a Home Monitoring System

• Registration Number: NCT01154205
• Lead Sponsor: Sheba Medical Center

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: 2010-06
• Study Start: 2010-06
• Study First Submitted: 2010-06-29
• Study First Submitted QC: 2010-06-29
• Last Update Submitted: 2010-06-29
• Study First Posted: 2010-06-30
• Last Update Posted: 2010-06-30
• Study Completion: 2012-01

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 100

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)

Sheba Medical Center; 🇮🇱 Tel HaShomer, Ramat Gan, Israel