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Ventricular Asynchrony in Cardiac Surgery Patients
This study is currently recruiting participants.
Verified by Weill Medical College of Cornell University, April 2008
First Received: April 1, 2008   No Changes Posted
Sponsored by: Weill Medical College of Cornell University
Information provided by: Weill Medical College of Cornell University
ClinicalTrials.gov Identifier: NCT00654199
  Purpose

The purpose of this study is to:

  1. assess the existence of inter-ventricular and intra-ventricular asynchrony in cardiac surgery patients before (PRE) and after cardiopulmonary bypass surgery (POST)
  2. investigate whether a modification of usual pacing practices (RA-LV pacing) can achieve inter- and intra-ventricular synchrony and improve heart function, as evaluated by hemodynamic and echocardiographic indexes, when compared with the patient's native rhythm (normal sinus rhythm (SR), or conventional pacing modes

Condition
Ventricular Asynchrony in Cardiac Surgery Patients

MedlinePlus related topics: Heart Surgery Surgery
U.S. FDA Resources
Study Type: Observational
Study Design: Case-Only, Prospective
Official Title: Ventricular Asynchrony in Cardiac Surgery Patients

Further study details as provided by Weill Medical College of Cornell University:

Biospecimen Retention:   None Retained

Biospecimen Description:

Estimated Enrollment: 20
Study Start Date: May 2006
Estimated Study Completion Date: October 2009
Estimated Primary Completion Date: May 2009 (Final data collection date for primary outcome measure)
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Inpatient population

Criteria

Inclusion Criteria:

  • scheduled for cardiac surgery, in normal sinus rhythm

Exclusion Criteria:

  • atrial fibrillation, abnormal hearth rhythms
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00654199

Contacts
Contact: Meg Kane, BA 212.746.2428 mek2007@med.cornell.edu
Contact: kathryn Koval, BA 212.746.2952 kak2006@med.cornell.edu

Locations
United States, New York
Weill Cornell Medical College Recruiting
New York, New York, United States, 10065
Contact: Meg Kane, BA     212-746-2428     mek2007@med.cornell.edu    
Contact: Kate Koval, BA     212.746.2952     kak2006@med.cornell.edu    
Principal Investigator: Nikolaos Skubas, MD            
Sponsors and Collaborators
Weill Medical College of Cornell University
  More Information

No publications provided

Responsible Party: Weill Cornell Medical College ( Nikolaos Skubas, MD )
Study ID Numbers: 0507007970
Study First Received: April 1, 2008
Last Updated: April 1, 2008
ClinicalTrials.gov Identifier: NCT00654199     History of Changes
Health Authority: United States: Weill Cornell Medical College IRB

Keywords provided by Weill Medical College of Cornell University:
CABG
Ventricular Asynchrony
Normal Sinus Rhythm

ClinicalTrials.gov processed this record on May 07, 2009