Monaldi Hospital Rhythm Registry
Registry of Patients Underwent Cardiac Implanted Electronic Device Implantation at Monaldi Hospital
University of Campania Luigi Vanvitelli
5,000 participants
Jan 7, 2015
OBSERVATIONAL
Conditions
Summary
The study is a prospective registry. Consecutive patients with indications of implant / replacement or upgrade of pacemaker (PM), implantable cardioverter defibrillator (ICD), Implanted loop recorder (ILR) will be enrolled. The primary objective of the study is to describe the clinical events during a long-term follow-up of non-selected population of patients implanted with an PM, ICD or ILR.
Eligibility
Inclusion Criteria3
- All consecutive patients underwent PM/ICD/ILR implantation
- Patient is willing and able to sign an authorization to use and disclose health information or an Informed Consent
- Patient must be able to attend all required follow-up visits at the study center for at least 12 months
Exclusion Criteria3
- No informed consent
- Patient is participating in another clinical study that may have an impact on the study endpoint
- No informed consent
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Interventions
Implantation of single chamber, dual chambers or triple chambers PM/ICD
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT05072119