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Prophylactic Pulmonary Vein Isolation Study

Primary Purpose

Atrial Fibrillation

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Pulmonary Vein Isolation
Sponsored by
Mayo Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Atrial Fibrillation focused on measuring Atrial Fibrillation, AF, A fib, cardiac ablation, modified maze procedure

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Indication for open-heart surgery: Mitral valve repair or replacement, evidence of a dilated left atrium

Exclusion Criteria:

  • History of Atrial Fibrillation
  • Need for emergent cardiac surgery
  • Previous cardiac surgery
  • Preoperative need for an intraaortic balloon pump or intravenous inotropes
  • Current diagnosis of active endocarditis
  • Mental impairment/or experience other conditions which may not allow subject to understand nature
  • Significance and scope of study
  • Pregnancy

Sites / Locations

  • Mayo Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

No Intervention

Arm Label

1

2

Arm Description

The treatment group will undergo operation for mitral valve disease with an additional procedure called Pulmonary Vein Isolation.

The control group of patients will undergo operation for mitral valve disease without the additional Pulmonary Vein Isolation

Outcomes

Primary Outcome Measures

Evaluated by the number of patients free of taking antiarrhythmic medications and free of AF as determined by a 24-hour Holter recording.

Secondary Outcome Measures

Full Information

First Posted
December 22, 2007
Last Updated
April 12, 2011
Sponsor
Mayo Clinic
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1. Study Identification

Unique Protocol Identification Number
NCT00587899
Brief Title
Prophylactic Pulmonary Vein Isolation Study
Official Title
A Randomized, Single-blind Prophylactic Pulmonary Vein Isolation Procedure Utilizing Bipolar Radiofrequency Ablation in Patients Undergoing Mitral Valve Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
April 2011
Overall Recruitment Status
Terminated
Why Stopped
enrollment has been lower than anticipated due to growth in the minimally invasive mitral valve repair practice.
Study Start Date
January 2007 (undefined)
Primary Completion Date
November 2009 (Actual)
Study Completion Date
November 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Mayo Clinic

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study is being done to learn the effects of the Pulmonary Vein Isolation in patients that are at high risk to developing, but do not have a documented history of atrial fibrillation.
Detailed Description
Patients with a dilated left atrium (left upper chamber of the heart) that undergo mitral valve surgery may be at risk for the development of atrial fibrillation after surgery. Atrial fibrillation (also known as "A-Fib" or AF) is an abnormal heart rhythm which may cause symptoms such as pounding sensations in your chest, dizziness, fatigue, chest pain and/or shortness of breath. AF patients are at a higher risk of developing a stroke. Participants who sign informed consent will be randomized into one of two groups by chance (as in the flip of a coin). Approximately 77 patients will undergo their mitral valve operation along with Pulmonary Vein Isolation (a treatment group) and 77 patients who do not undergo Pulmonary Vein Isolation at the time of their mitral valve surgery (a control group). The treatment group will undergo operation for mitral valve disease with an additional procedure called Pulmonary Vein Isolation using a device that delivers radiofrequency energy to the heart muscle in order to create scar tissue to block electrical impulses that can trigger episodes of AF. The control group of patients will undergo operation for mitral valve disease without the additional Pulmonary Vein Isolation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Fibrillation
Keywords
Atrial Fibrillation, AF, A fib, cardiac ablation, modified maze procedure

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
41 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Other
Arm Description
The treatment group will undergo operation for mitral valve disease with an additional procedure called Pulmonary Vein Isolation.
Arm Title
2
Arm Type
No Intervention
Arm Description
The control group of patients will undergo operation for mitral valve disease without the additional Pulmonary Vein Isolation
Intervention Type
Procedure
Intervention Name(s)
Pulmonary Vein Isolation
Intervention Description
The treatment group will undergo operation for mitral valve disease with an additional procedure called Pulmonary Vein Isolation using a device that delivers radiofrequency energy to the heart muscle in order to create scar tissue to block electrical impulses that can trigger episodes of AF.
Primary Outcome Measure Information:
Title
Evaluated by the number of patients free of taking antiarrhythmic medications and free of AF as determined by a 24-hour Holter recording.
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Indication for open-heart surgery: Mitral valve repair or replacement, evidence of a dilated left atrium Exclusion Criteria: History of Atrial Fibrillation Need for emergent cardiac surgery Previous cardiac surgery Preoperative need for an intraaortic balloon pump or intravenous inotropes Current diagnosis of active endocarditis Mental impairment/or experience other conditions which may not allow subject to understand nature Significance and scope of study Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thoralf M. Sundt, III, M.D.
Organizational Affiliation
Professor of Surgery, Mayo Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55902
Country
United States

12. IPD Sharing Statement

Links:
URL
http://clinicaltrials.mayo.edu
Description
Mayo Clinic Clinical Trials

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Prophylactic Pulmonary Vein Isolation Study

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