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

This study has been completed.

First Received on February 14, 2006. Last Updated on April 22, 2009 History of Changes

Sponsor:	Guidant Corporation
Information provided by:	Guidant Corporation
ClinicalTrials.gov Identifier:	NCT00292539

Purpose

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.

Condition	Intervention
Atrial Fibrillation Bradycardia Heart Block Sick Sinus Syndrome	Device: Any pacemaker with right ventricular pacing option

Study Type:	Observational
Study Design:	Observational Model: Cohort Time Perspective: Retrospective
Official Title:	Preserve Registry: Prospective Registry of Pacemaker Patients Concerning Percentage of Right Ventricular Pacing, LVEF and NYHA Class

Resource links provided by NLM:

Genetics Home Reference related topics: Brugada syndrome familial atrial fibrillation short QT syndrome

MedlinePlus related topics: Atrial Fibrillation

U.S. FDA Resources

Further study details as provided by Guidant Corporation:

Estimated Enrollment:	600
Study Start Date:	February 2006
Study Completion Date:	September 2006

Eligibility

Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

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

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00292539

Locations

Germany
Kreiskrankenhaus
Viechtach, Germany, 94234

Sponsors and Collaborators

Guidant Corporation

Investigators

Study Director:

Sven Treusch, PHD

Guidant Corporation

More Information

No publications provided

Responsible Party:	Sven Treusch, Guidant Germany
ClinicalTrials.gov Identifier:	NCT00292539 History of Changes
Other Study ID Numbers:	Preserve Registry
Study First Received:	February 14, 2006
Last Updated:	April 22, 2009
Health Authority:	Germany: Federal Institute for Drugs and Medical Devices

Keywords provided by Guidant Corporation:

Pacemaker
NYHA class
Ejection fraction
Heart Failure

Additional relevant MeSH terms:

Atrial Fibrillation
Heart Block
Sick Sinus Syndrome
Bradycardia
Arrhythmias, Cardiac

Heart Diseases
Cardiovascular Diseases
Pathologic Processes
Arrhythmia, Sinus

ClinicalTrials.gov processed this record on February 09, 2012