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

NCT ID: NCT01138670

Last Updated: 2012-11-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

5500 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-05-31

Study Completion Date

2014-12-31

Brief Summary

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

Detailed Description

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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.

Conditions

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Pacemaker Defibrillators, Implantable

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Cardiac device group

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

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

Exclusion Criteria

* none
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Aarhus

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Rikke E Kirkfeldt, MD

Role: PRINCIPAL_INVESTIGATOR

Aarhus Universitetshospital, Skejby

Locations

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Aarhus Universitetshospital, Skejby

Aarhus, , Denmark

Site Status

Countries

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Denmark

Other Identifiers

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SKS-REK-2

Identifier Type: -

Identifier Source: org_study_id