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Atrial Fibrillation: Ablation or Surgical Treatment II: FAST II

Primary Purpose

Paroxysmal Atrial Fibrillation.

Status
Terminated
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Percutaneous radiofrequency catheter ablation
Mini invasive thoracoscopic radiofrequency ablation
Sponsored by
Aalborg University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Paroxysmal Atrial Fibrillation. focused on measuring Percutaneous radiofrequency catheter ablation, Mini invasive thoracoscopic radiofrequency ablation

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Recurrent symptomatic paroxysmal atrial fibrillation
  • Previously failed one or more antiarrhythmic or beta-blocker medication (treatment > 30 days) or if any contraindications against treatment with these drug.
  • Patient is willing and able to attend the scheduled follow-up visits
  • Signed informed consent

Exclusion Criteria:

  • Persistent or permanent atrial fibrillation
  • Previously atrial fibrillation ablation procedure
  • Atrial fibrillation secondary to electrolyte imbalance, thyroid disease, or reversible or non-cardiac cause
  • Severe underlying heart disease (congenital heart disease, significant valvular disease, cardiomyopathy with LVEF < 35 %, angina pectoris/ ischemic heart disease).
  • Severe enlargement of left atrium (> 45mm)
  • Patient with pacemaker
  • Failure to obtain informed consent
  • Pregnant or breastfeeding women.
  • Patient unable to undergo TEE or with documented left atrial thrombus
  • Patients with co-morbid conditions who, in the opinion of the investigator, constitute increased risk of general anesthesia or port access, e.g. pleural fibrosis, chronic obstructive pulmonary disease (FEV1 < 1.5 L/s).
  • Known internal carotid artery stenosis (> 80 %).
  • Patients, who are enrolled in another clinical trial
  • Life expectancy less than one year
  • Previously TIA/stroke

Sites / Locations

  • Dept of Cardiothoracic surgery and Dept of Cardiology, Aalborg Hospital
  • Odense Universityhospital
  • St. Antonius Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Mini invasive thoracoscopic radiofrequency ablation

Percutaneous ablation

Arm Description

Video-assisted thoracoscopic radiofrequency ablation

Percutaneous radiofrequency catheter ablation

Outcomes

Primary Outcome Measures

Freedom from atrial fibrillation with or without antiarrhythmic drug.
Determined by seven days Holter monitoring, ECG, and patient interviews. An episode of atrial fibrillation/flutter/tachycardia is defined as more than 30 seconds of atrial fibrillation observed on Holter monitoring/telemetry or ECG

Secondary Outcome Measures

Quality of life
Comparison of quality of life before ablation and at follow-up, by 4 different quality of life questionnaires AFEQT, AF-QoL-18, GAD-7 and PHQ-9.
Procedural complications
Thromboembolic events (TIA,Stroke), Mortality, Tamponade, need for thoracotomy, bleeding, infection, esophageal fistula, embolic events, death , pneumothorax and hemothorax.
Health economics (cost-effectiveness analysis)
Reduction in atrial fibrillation burden

Full Information

First Posted
April 13, 2011
Last Updated
January 2, 2014
Sponsor
Aalborg University Hospital
Collaborators
St. Antonius Hospital, Odense University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01336075
Brief Title
Atrial Fibrillation: Ablation or Surgical Treatment II: FAST II
Official Title
Atrial Fibrillation: Ablation or Surgical Treatment II: FAST II A Randomized Study Comparing Non-pharmacologic Therapy in Patients With Drug-refractory Atrial Fibrillation Referred for a First Time Invasive Treatment.
Study Type
Interventional

2. Study Status

Record Verification Date
January 2014
Overall Recruitment Status
Terminated
Why Stopped
Too few participants
Study Start Date
April 2011 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
December 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Aalborg University Hospital
Collaborators
St. Antonius Hospital, Odense University Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to compare two invasive treatments of symptomatic paroxysmal atrial fibrillation: Percutaneous radiofrequency catheter ablation and mini invasive thoracoscopic radiofrequency ablation in patients referred for a first time invasive treatment for atrial fibrillation. The hypothesis is, that mini invasive thoracoscopic radiofrequency ablation as a first time invasive treatment is more effective compared to a percutaneous catheter based technique in patients with symptomatic paroxysmal atrial fibrillation refractory or intolerant to at least one antiarrhythmic drug.
Detailed Description
Atrial fibrillation is characterized by disorganized, rapid, and irregular contraction of the atria. Its effects on hemodynamic and thromboembolic events result in significant morbidity, mortality, impaired quality of life, hospitalizations, and health-cost. It is the most common sustained cardiac arrhythmia. Over six million Europeans suffer from this arrhythmia. The prevalence is estimated to at least double in the next 50 years and is probably underestimated due to asymptomatic atrial fibrillation. The prevalence increases with age and affects men more often. Atrial fibrillation is treated medically with varying results and there are no definitive long term curative treatments. The main goal aims at reducing symptoms and preventing disabling complications. Treatment normally includes antithrombotic, rhythm, and/or rate management, New non-pharmacological interventions have evolved over the last decades in order to prevent paroxysmal atrial fibrillation and/or reduce symptoms. The main focus of non-pharmacological intervention has been on percutaneous radiofrequency catheter ablation and surgical maze ablation. Both approaches aim at minimizing the impact of "triggers" from the pulmonary veins by electrical isolation of the veins. Studies comparing antiarrhythmic drug and radiofrequency ablation indicate that radiofrequency ablation has a higher efficacy rate, a lower rate of complications, and in selected patients radiofrequency ablation reduced the risk of atrial fibrillation recurrence after one year by 65 % compared with antiarrhythmic drug. In a recently published paper the success rate after a mean of 1.3 radiofrequency ablation procedures per patient varied from 57.7% to 75.4% with higher success rates in patients with paroxysmal atrial fibrillation as compared to persistent/permanent atrial fibrillation. European Society of Cardiology recommends that radiofrequency ablation is reserved for patients who remain symptomatic despite optimal therapy and failed at least one antiarrhythmic drug. Dr. James Cox introduced the Cox-maze surgical operation for atrial fibrillation in 1987, later modified to Cox-maze III also known as the "cut and sew" maze. It is highly successful in restoring sinus rhythm, with 90-96 % being free from atrial fibrillation at a mean follow-up of 5.4 years. Due to its complexity and technical difficulty the procedure has not been widely adopted. Mini invasive procedures for pulmonary vein isolation have been developed and can now be performed either through mini thoracotomies or using totally thoracoscopic approach. These procedures also hold the advantage of left atrial appendage excision or exclusion. The thoracoscopic maze ablation has shown promising results in small studies in patients with recurrence of atrial fibrillation after earlier catheter based radiofrequency ablation, after a mean follow-up of 11 months 84 % of the patients remain in sinus rhythm. However long-term results are still unknown. The procedure still needs to be compared head to head with catheter based radiofrequency ablation before it should be offered as a standard treatment of atrial fibrillation. The rationale for eliminating atrial fibrillation with radiofrequency ablation include a potential improvement in quality of life, decreased stroke risk, decreased heart failure risk and improved survival.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Paroxysmal Atrial Fibrillation.
Keywords
Percutaneous radiofrequency catheter ablation, Mini invasive thoracoscopic radiofrequency ablation

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Mini invasive thoracoscopic radiofrequency ablation
Arm Type
Active Comparator
Arm Description
Video-assisted thoracoscopic radiofrequency ablation
Arm Title
Percutaneous ablation
Arm Type
Active Comparator
Arm Description
Percutaneous radiofrequency catheter ablation
Intervention Type
Procedure
Intervention Name(s)
Percutaneous radiofrequency catheter ablation
Other Intervention Name(s)
Radiofrequency ablation, Catheter ablation, Atrial fibrillation ablation
Intervention Description
Percutaneous radiofrequency catheter ablation around the rights and lefts pulmonary veins, with complete circumferential ablation.
Intervention Type
Procedure
Intervention Name(s)
Mini invasive thoracoscopic radiofrequency ablation
Other Intervention Name(s)
Mini invasive mini maze
Intervention Description
Video-assisted thoracoscopic approach for electrical isolation of the pulmonary veins bilaterally and left atrial appendage excision or exclusion.
Primary Outcome Measure Information:
Title
Freedom from atrial fibrillation with or without antiarrhythmic drug.
Description
Determined by seven days Holter monitoring, ECG, and patient interviews. An episode of atrial fibrillation/flutter/tachycardia is defined as more than 30 seconds of atrial fibrillation observed on Holter monitoring/telemetry or ECG
Time Frame
12 month follow-up
Secondary Outcome Measure Information:
Title
Quality of life
Description
Comparison of quality of life before ablation and at follow-up, by 4 different quality of life questionnaires AFEQT, AF-QoL-18, GAD-7 and PHQ-9.
Time Frame
12 month follow-up
Title
Procedural complications
Description
Thromboembolic events (TIA,Stroke), Mortality, Tamponade, need for thoracotomy, bleeding, infection, esophageal fistula, embolic events, death , pneumothorax and hemothorax.
Time Frame
12 month follow-up
Title
Health economics (cost-effectiveness analysis)
Time Frame
12 month follow-up
Title
Reduction in atrial fibrillation burden
Time Frame
12 month follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Recurrent symptomatic paroxysmal atrial fibrillation Previously failed one or more antiarrhythmic or beta-blocker medication (treatment > 30 days) or if any contraindications against treatment with these drug. Patient is willing and able to attend the scheduled follow-up visits Signed informed consent Exclusion Criteria: Persistent or permanent atrial fibrillation Previously atrial fibrillation ablation procedure Atrial fibrillation secondary to electrolyte imbalance, thyroid disease, or reversible or non-cardiac cause Severe underlying heart disease (congenital heart disease, significant valvular disease, cardiomyopathy with LVEF < 35 %, angina pectoris/ ischemic heart disease). Severe enlargement of left atrium (> 45mm) Patient with pacemaker Failure to obtain informed consent Pregnant or breastfeeding women. Patient unable to undergo TEE or with documented left atrial thrombus Patients with co-morbid conditions who, in the opinion of the investigator, constitute increased risk of general anesthesia or port access, e.g. pleural fibrosis, chronic obstructive pulmonary disease (FEV1 < 1.5 L/s). Known internal carotid artery stenosis (> 80 %). Patients, who are enrolled in another clinical trial Life expectancy less than one year Previously TIA/stroke
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Henrik Vadmann, MD
Organizational Affiliation
Aalborg University Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sam Riahi, MD, PhD
Organizational Affiliation
Aalborg University Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jan Jesper Andreasen, MD, PhD
Organizational Affiliation
Aalborg University Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Søren Hjortshøj, MD, PhD
Organizational Affiliation
Aalborg University Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Alaaddin Yilmaz, MD
Organizational Affiliation
St. Antonius Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Lucas Boersma, MD, PhD
Organizational Affiliation
St. Antonius Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Axel Brandes, MD, FESC
Organizational Affiliation
Odense Universityhospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Peter Pallesen, MD
Organizational Affiliation
Odense Universityhospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dept of Cardiothoracic surgery and Dept of Cardiology, Aalborg Hospital
City
Aalborg
ZIP/Postal Code
9000
Country
Denmark
Facility Name
Odense Universityhospital
City
Odense
ZIP/Postal Code
5000
Country
Denmark
Facility Name
St. Antonius Hospital
City
Nieuwegein
ZIP/Postal Code
3430
Country
Netherlands

12. IPD Sharing Statement

Citations:
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20876603
Citation
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derived

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Atrial Fibrillation: Ablation or Surgical Treatment II: FAST II

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