Implantable Cardiac Device Long Term Observational study (Panorama OS)
Phase 4
Completed
- Conditions
- Health Condition 1: null- Patients to be implanted with a Medtronic market-released cardiac devices (IPG, ICD).
- Registration Number
- CTRI/2009/091/000420
- Lead Sponsor
- Medtronic Bakken Research Centre Endepolsdomein GW MaastrichtThe Netherlands
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 10000
Inclusion Criteria
1. Any patient (to be) implanted with a Medtronic market-released cardiac device is eligible.
2. Signed Patient Data Release Form.
Exclusion Criteria
1. Unwillingness or inability to cooperate or give voluntary consent to participate.
2. Enrollment outside a 30-day window from the planned/perfromed implant procedure.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Epidemiological databaseTimepoint: 1 year after implant
- Secondary Outcome Measures
Name Time Method Epidemiological databaseTimepoint: 1 year after implant