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Complications Following Pacemaker or Implantable Defibrillator Cardioverter (ICD) Implantation in Denmark

Conditions
Pacemaker
Defibrillators, Implantable
Registration Number
NCT01138670
Lead Sponsor
University of Aarhus
Brief Summary

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

Detailed 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.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
5500
Inclusion Criteria
  • patients receiving a cardiac device (pacemaker, cardiac resynchronization therapy (CRT) or implantable defibrillator cardioverter (ICD)), or undergoing a reoperation
Exclusion Criteria
  • none

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
complication rate3 months

any complication that require treatment There is no 'Safety and Tolerability' or 'Pain' measurement.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Aarhus Universitetshospital, Skejby

🇩🇰

Aarhus, Denmark

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