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

Complications Following Pacemaker or ICD Implantation in Denmark

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01138670

Enrollment

5500

Registered

2010-06-07

Start date

2010-05-31

Completion date

2014-12-31

Last updated

2012-11-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Defibrillators, Implantable, Pacemaker

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.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Healthy volunteers

Inclusion criteria

* patients receiving a cardiac device (pacemaker, cardiac resynchronization therapy (CRT) or implantable defibrillator cardioverter (ICD)), or undergoing a reoperation

Exclusion criteria

* none

Design outcomes

Primary

Measure	Time frame	Description
complication rate	3 months	any complication that require treatment There is no 'Safety and Tolerability' or 'Pain' measurement.

Countries

Denmark

Outcome results