Prospective Registry of Pacemaker Patients Concerning Percentage of Right Ventricular Pacing, LVEF and NYHA Class

This study has been completed.
Sponsor:
Information provided by:
Guidant Corporation
ClinicalTrials.gov Identifier:
NCT00292539
First received: February 14, 2006
Last updated: April 22, 2009
Last verified: April 2009

February 14, 2006
April 22, 2009
February 2006
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Complete list of historical versions of study NCT00292539 on ClinicalTrials.gov Archive Site
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Prospective Registry of Pacemaker Patients Concerning Percentage of Right Ventricular Pacing, LVEF and NYHA Class
Preserve Registry: Prospective Registry of Pacemaker Patients Concerning Percentage of Right Ventricular Pacing, LVEF and NYHA Class

This registry is a data collection on patients who are implanted for more than 6 months with a pacemaker. Frequency and distribution of right ventricular pacing, NYHA class and left ventricular ejection fraction shall be documented.

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Observational
Observational Model: Cohort
Time Perspective: Retrospective
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  • Atrial Fibrillation
  • Bradycardia
  • Heart Block
  • Sick Sinus Syndrome
Device: Any pacemaker with right ventricular pacing option
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
600
September 2006
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Inclusion Criteria:

  • Implanted pacemaker for more than 6 months, VVI/DDD, written consent

Exclusion Criteria:

  • Pacemaker implanted for less than 6 months, no right ventricular pacing possibility (AAI), no consent
Both
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No
Contact information is only displayed when the study is recruiting subjects
Germany
 
NCT00292539
Preserve Registry
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Sven Treusch, Guidant Germany
Guidant Corporation
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Study Director: Sven Treusch, PHD Guidant Corporation
Guidant Corporation
April 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP