View Clinical Trial (Medical Research Study)
Bipolar Radiofrequency Ablation -Role in Prevention of Postoperative Atrial Fibrillation - NCT00765089-15102(Clinical Trial 244399)
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Pittsburgh |
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State:
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PA |
| Zip Code: |
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15102 |
| Conditions: |
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Postoperative Atrial Fibrillation |
| Purpose: |
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Atrial Fibrillation (AF) is one of the most common postoperative complications after
coronary artery bypass grafting (CABG). Postoperative AF produces a substantial impact on
hospital resources with an estimated annual expenditure of over $1 billion. This includes
the cost of pharmacological treatment and the cost of the increased length of stay. The
incidence of AF is about 30-40% in CABG patients and increases with age of the patient. As
the average age of the patient that undergoes CABG surgery is increasing, it is critical to
find a way to prevent or reduce the incidence of this complication.
We propose a prospective, randomized, controlled study to determine the role of pulmonary
vein isolation by bipolar ablation in the prevention or reduction of postoperative AF. The
block- randomization plan will be used to maintain balance of the study and control arms
throughout the study.
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| Study summary: |
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| Criteria: |
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Inclusion Criteria:
1. Patients who require an isolated elective CABG surgery on CPB.
2. Both male and female patients of age 18 years to 90 years.
Exclusion Criteria:
1. Pre existing atrial fibrillation or history of previous atrial fibrillation.
2. Inability to provide informed consent.
3. Pregnant or nursing patients.
4. Reoperative sternotomy
5. Emergency CABG surgery. |
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| Study is available at: |
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University of Pittsburgh Medical Center Pittsburgh, PA 15102 United States
Primary Contact: Sujatha Raghu, MBBS MPH Phone: 412-647-0749
Secondary Contact: Sujatha Raghu, MBBS MPH Email: raghus@upmc.edu Phone: 412-647-0749 |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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March 22, 2011 |
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