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CatHeter Ablation of perSistEnd Atrial Fibrillation: Pulmonary Vein Isolation Versus Defragmentation. The CHASE-AF Study (CHASE-AF)

Primary Purpose

Atrial Fibrillation, Persistent Atrial Fibrillation

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
PVI alone
PVI + Defragmentation + linear lesions
Sponsored by
Universitätsklinikum Hamburg-Eppendorf
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atrial Fibrillation

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age > 18
  • Persistent atrial fibrillation > 7 days or previous cardioversion
  • Obtained written consent

Exclusion Criteria:

  • Age less than 18 years
  • Previous operative or interventional treatment of atrial fibrillation
  • Paroxysmal atrial fibrillation
  • Pregnancy
  • Contraindication for oral anticoagulation
  • Contraindication for heparin administration
  • Transient factors causing atrial fibrillation (e.g. Hyperthyroidism)
  • Drug and alcohol abuse
  • Severe underlying heart disease with left atrial enlargement > 60 mm

Sites / Locations

  • University Hospital Eppendorf

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

PVI alone

PVI + Defragmentation + linear lesions

Arm Description

Pulmonary vein isolation alone in persistent atrial fibrillation

AF ablation continuation aiming for AF termination

Outcomes

Primary Outcome Measures

Recurrence of atrial arrhythmia during 12 months follow up

Secondary Outcome Measures

Number of periprocedural complications

Full Information

First Posted
April 16, 2012
Last Updated
April 28, 2019
Sponsor
Universitätsklinikum Hamburg-Eppendorf
Collaborators
Abbott Medical Devices
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1. Study Identification

Unique Protocol Identification Number
NCT01580124
Brief Title
CatHeter Ablation of perSistEnd Atrial Fibrillation: Pulmonary Vein Isolation Versus Defragmentation. The CHASE-AF Study
Acronym
CHASE-AF
Official Title
CatHeter Ablation of perSistEnd Atrial Fibrillation: Pulmonary Vein Isolation Versus Defragmentation. The CHASE-AF Study.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
November 2010 (undefined)
Primary Completion Date
February 2014 (Actual)
Study Completion Date
February 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universitätsklinikum Hamburg-Eppendorf
Collaborators
Abbott Medical Devices

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Study design: Randomized prospective comparison of pulmonary vein isolation alone versus a strategy aiming for atrial fibrillation termination by using a stepwise approach consisting of pulmonary vein isolation, biatrial defragmentation aiming for fractionated electrograms and linear ablation if required.
Detailed Description
Study protocol: In patients randomized to PVI alone, the index procedure consists of wide circumferential pulmonary vein isolation (1 cm distal of the PV ostium) including optional right atrial isthmus ablation. Endpoint for PVI is entrance block as evaluated by a circumferential mapping catheter during sinus rhythm at the end of the procedure. In all patients the NavX® three-dimensional mapping system should be used. The St. Jude Medical Coolflex® or Coolpath® catheters may be used at the operator's discretion. In patients randomized to the strategy aiming for atrial fibrillation termination PVI is also the initial step of the procedure followed by atrial defragmentation and eventual linear ablation in case of atrial tachycardia aiming for acute restoration of sinus rhythm. The procedural steps with regard to mapping and ablation of atrial fibrillation and consecutive atrial tachycardia follow the previously described methods (8,9). After initial ablation the previous antiarrhythmic drug treatment can be continued but no de novo antiarrhythmic drug regiment should be applied. The primary endpoint of this study is recurrence of atrial arrhythmias between 6 and 12 months after the initial ablation procedure. In both study arms, the same CE certified catheters will be used. Usually, the setting consists of on decapolar catheter positioned in the coronary sinus, one circumferential mapping catheters for mapping of the pulmonary veins, one quadripolar catheter for mapping the right atrium. In both study groups a externally irrigated catheter for mapping and ablation will be used (CoolFlex/ Coolpath as mentioned above). Sample size calculation: According to the assumption of a difference of 30 % regarding the primary endpoint (power 80, alpha=0.05) 70 patients have to be included. Considering a potential drop out of 10 % 160 patients should be included. However, an adaptive statistical plan is applied (Prof. Wegscheider, University Hospital Hamburg). Follow up and repeat procedures: Crossover between the two treatment options should be avoided. Previous antiarrhythmic drug treatment can be continued until month 6 after the index procedure is completed. Repeat procedures between month 0 and 3 should be avoided. Repeat procedures should be planned between month 3 and 6 after the index procedure. The initial approach of the repeat procedure is the same as during the index procedure (Figure 1). Thus, in patients randomized for PVI alone, PVI will be repeated in case of reconnection of the veins. In the setting of complete block of all pulmonary veins also patients randomized to PVI alone will receive a substrate modification as in the other group. Patients randomized to the ablation procedure aiming for AF termination will again receive a 'complete' procedure including assessment of PVI and ablation of atrial tachycardias and atrial fibrillation. Follow-up: All patients will be seen in the outpatient clinic every 3 month during the 12 month study period. The visit will include ECG and Holter ECG recordings. Additionally, echocardiography and interrogation of pacemaker will be performed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Fibrillation, Persistent Atrial Fibrillation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
150 (Actual)

8. Arms, Groups, and Interventions

Arm Title
PVI alone
Arm Type
Active Comparator
Arm Description
Pulmonary vein isolation alone in persistent atrial fibrillation
Arm Title
PVI + Defragmentation + linear lesions
Arm Type
Active Comparator
Arm Description
AF ablation continuation aiming for AF termination
Intervention Type
Procedure
Intervention Name(s)
PVI alone
Intervention Description
PVI alone Pulmonary vein isolation alone in persistent atrial fibrillation
Intervention Type
Procedure
Intervention Name(s)
PVI + Defragmentation + linear lesions
Intervention Description
PVI + Defragmentation + linear lesions AF ablation continuation aiming for AF termination
Primary Outcome Measure Information:
Title
Recurrence of atrial arrhythmia during 12 months follow up
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Number of periprocedural complications
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > 18 Persistent atrial fibrillation > 7 days or previous cardioversion Obtained written consent Exclusion Criteria: Age less than 18 years Previous operative or interventional treatment of atrial fibrillation Paroxysmal atrial fibrillation Pregnancy Contraindication for oral anticoagulation Contraindication for heparin administration Transient factors causing atrial fibrillation (e.g. Hyperthyroidism) Drug and alcohol abuse Severe underlying heart disease with left atrial enlargement > 60 mm
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stephan Willems, MD
Organizational Affiliation
University Heart Center Hamburg
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Daniel Steven, MD
Organizational Affiliation
University Heart Center Hamburg
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Eppendorf
City
Hamburg
ZIP/Postal Code
20251
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
26700836
Citation
Vogler J, Willems S, Sultan A, Schreiber D, Luker J, Servatius H, Schaffer B, Moser J, Hoffmann BA, Steven D. Pulmonary Vein Isolation Versus Defragmentation: The CHASE-AF Clinical Trial. J Am Coll Cardiol. 2015 Dec 22;66(24):2743-2752. doi: 10.1016/j.jacc.2015.09.088.
Results Reference
derived
Links:
URL
https://www.ncbi.nlm.nih.gov/pubmed/26700836
Description
PubMed

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CatHeter Ablation of perSistEnd Atrial Fibrillation: Pulmonary Vein Isolation Versus Defragmentation. The CHASE-AF Study

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