Overview

This trial is active, not recruiting.

Conditions pacemaker, defibrillators, implantable
Sponsor University of Aarhus
Start date May 2010
End date December 2013
Trial size 5500 participants
Trial identifier NCT01138670, SKS-REK-2

Summary

This study examines possible risk factors with regard to complications following pacemaker or implantable defibrillator cardioverter (ICD) implantation.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Observational model cohort
Time perspective prospective
Arm

Primary Outcomes

Measure
complication rate
time frame: 3 months

Eligibility Criteria

Male or female participants of any age.

Inclusion Criteria: - patients receiving a cardiac device (pacemaker, cardiac resynchronization therapy (CRT) or implantable defibrillator cardioverter (ICD)), or undergoing a reoperation Exclusion Criteria: - none

Additional Information

Official title Complications Following Pacemaker or ICD Implantation in Denmark
Principal investigator Rikke E Kirkfeldt, MD
Description This study examines possible risk factors with regard to complications following pacemaker or implantable defibrillator cardioverter (ICD)implantation. Furthermore validation af the Danish Pacemaker and ICD Register will be conducted.
Trial information was received from ClinicalTrials.gov and was last updated in November 2012.
Information provided to ClinicalTrials.gov by University of Aarhus.