Viewing Study NCT03612635


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Study NCT ID: NCT03612635
Status: COMPLETED
Last Update Posted: 2018-08-02
First Post: 2018-07-19
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Impact on Patient Outcome of Cardiac Implantable Electronic Device Complications
Sponsor: Azienda Ospedaliera Cardinale G. Panico
Organization:

Study Overview

Official Title: Impact on Patient Outcome and Healthcare Utilization of Cardiac ImplaNTable Electronic Devices Complications
Status: COMPLETED
Status Verified Date: 2018-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: POINTED
Brief Summary: The purpose of this registry is to evaluate the impact on patient outcome and on healthcare utilization of cardiac implantation electronic device complications during a long-term follow-up.
Detailed Description: Multicentric, observational, prospective registry enrolling consecutive patients underwent pacemaker or defibrillator implantation, aimed to evaluate the impact of cardiac implantable device complications requiring surgical revision on healthcare utilization (number and length of hospitalizations), and on patient outcome (all-cause mortality and cardiac mortality), during a long-term follow-up.

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: