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Placement of Permanent Pacemaker Study

NCT ID: NCT00512161

Last Updated: 2017-01-19

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

COMPLETED

Total Enrollment

500 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-06-30

Study Completion Date

2011-12-31

Brief Summary

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The purpose of this study is to determine the predictors for placement of permanent pacemakers soon after cardiac surgery. We will measure the following to see what influence, if any, they have on predicting the need for permanent pacemaker implantation.

1. Type of cardiac surgery
2. Gender of patient
3. Patient's age
4. Preoperative heart rhythm and rate
5. Duration on cardiopulmonary bypass
6. Immediate post cardiopulmonary bypass heart rhythm and rate.
7. All heart rhythms and rates identified in the postoperative period prior to permanent pacemaker implantation.
8. Underlying heart rhythm and rates when permanent pacemaker is placed.
9. Ejection fraction before surgery
10. Ejection fraction immediately post-cardiopulmonary bypass

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Detailed Description

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The purpose of this study is to determine the predictors for placement of permanent pacemakers soon after cardiac surgery. We will measure the following to see what influence, if any, they have on predicting the need for permanent pacemaker implantation. Through investigation into the co-morbidities, diagnoses, or histories associated with an endpoint permanent pacemaker placement, it is possible that we will garner a better idea of who will require PPP.

Conditions

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Cardiac Surgical Procedures

Study Design

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Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* All patients between the ages of 18-99 years.
* All patients undergoing cardiac surgery requiring cardiopulmonary bypass.

Exclusion Criteria

* Patients who have permanent pacemakers in place.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Weill Medical College of Cornell University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Gregory E. Kerr, M.D., M.B.A.

Role: PRINCIPAL_INVESTIGATOR

Weill Medical College of Cornell University

John J. Savarese, M.D.

Role: STUDY_CHAIR

Weill Medical College of Cornell University

Locations

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Weill Medical College of Cornell University

New York, New York, United States

Site Status

Countries

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United States

Other Identifiers

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0701008942

Identifier Type: -

Identifier Source: org_study_id

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