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A Prospective Randomized Study Comparing Radiofrequency Energy With Cryoenergy (CRYO-RF)

Primary Purpose

Atrial Fibrillation Ablation

Status
Unknown status
Phase
Phase 4
Locations
Germany
Study Type
Interventional
Intervention
PVI using an open irrigated tip catheter
PVI using a closed irrigated tip catheter
PVI using a cryoballoon
Sponsored by
Herz-Zentrums Bad Krozingen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atrial Fibrillation Ablation focused on measuring atrial fibrillation, pulmonary veins, ablation

Eligibility Criteria

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

Inclusion Criteria:

  • Age between 18 and 75 years
  • Symptomatic drug refractory (more than 2 antiarrhythmic drugs) paroxysmal or persistent AF
  • Documentation of AF on 12 lead ECG and/ or Holter
  • Left atrium of less than 55 mm
  • Informed consent signed by the patient

Exclusion Criteria:

  • Previous Ablation or operation for AF
  • Contra-indication for heart catheterisation
  • Cardioversion for AF during the 2 weeks before the procedure

Sites / Locations

  • Herz-ZentrumRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

1

2

3

Arm Description

Outcomes

Primary Outcome Measures

Changes of platelet function (number of patients with an increase of more than 100% in platelets positive for either P-selectin or activated GP IIb/IIIa)

Secondary Outcome Measures

Parameters of inflammation and tissue damage, the time to achieve PV-Isolation, freedom from AF.

Full Information

First Posted
October 14, 2008
Last Updated
October 14, 2008
Sponsor
Herz-Zentrums Bad Krozingen
Collaborators
CryoCath Technologies Inc., Boston Scientific Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT00773539
Brief Title
A Prospective Randomized Study Comparing Radiofrequency Energy With Cryoenergy
Acronym
CRYO-RF
Official Title
Safety and Efficacy of Transvenous Pulmonary Isolation for the Treatment of Atrial Fibrillation: A Prospective Randomized Study Comparing Radiofrequency Energy With Cryoenergy
Study Type
Interventional

2. Study Status

Record Verification Date
October 2008
Overall Recruitment Status
Unknown status
Study Start Date
July 2008 (undefined)
Primary Completion Date
February 2009 (Anticipated)
Study Completion Date
August 2009 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Herz-Zentrums Bad Krozingen
Collaborators
CryoCath Technologies Inc., Boston Scientific Corporation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Transvenous pulmonary vein (PV) isolation using radiofrequency energy is an effective treatment for atrial fibrillation (1-4). However, rare but potentially life threatening complications such as thromboembolism (5), PV stenosis (5-10), left atrium-oesophageal fistula (11) and inflammatory syndromes (12) have been described. In preliminary studies an alternate approach using cryoenergy induces less endothelial disruption/ thrombus formation (13), preserves the extra cellular matrix and creates lesions with well-delineated border zones (14). Therefore, cryoenergy seems to be the ideal form of energy to safely perform PV isolation. We therefore hypothesise that in the setting of PV isolation for the treatment of atrial fibrillation (AF) cryoenergy is less traumatic and therefore reduces systemic inflammatory responses compared to radiofrequency energy. 78 patients presenting with symptomatic intermittent or persistent AF will be randomised to PV isolation with either radiofrequency (26 patients open irrigated tip, 26 patients closed irrigated tip) or cryoenergy (26 patients with cryoballoon). Systemic markers of cell damage and inflammatory response (t-troponin, CK, CK-MB, vWF, PAI-1, micro particles, platelet activation/overall function, CRP, IL-6, IL-8, IL-10, TNF alpha, procalcitonin) will be monitored before, during and 48h after the procedure. Further endpoints include time to PV-isolation and procedure related complications. Six month clinical follow-up will focus on freedom from AF and cardiovascular events.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Fibrillation Ablation
Keywords
atrial fibrillation, pulmonary veins, ablation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
78 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Title
2
Arm Type
Active Comparator
Arm Title
3
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
PVI using an open irrigated tip catheter
Intervention Description
transseptal PVI using thermocooled ablation catheter (Biosense) with confirmation of conduction block
Intervention Type
Procedure
Intervention Name(s)
PVI using a closed irrigated tip catheter
Intervention Description
transseptal PVI using the CHILLI II catheter from BOSTON with confirmation of conduction block
Intervention Type
Procedure
Intervention Name(s)
PVI using a cryoballoon
Intervention Description
transseptal PVI using the cryoballoon from CRYOCATH
Primary Outcome Measure Information:
Title
Changes of platelet function (number of patients with an increase of more than 100% in platelets positive for either P-selectin or activated GP IIb/IIIa)
Time Frame
before, at the end of intervention, 6, 24 and 48 hours later.
Secondary Outcome Measure Information:
Title
Parameters of inflammation and tissue damage, the time to achieve PV-Isolation, freedom from AF.
Time Frame
before, during and 6 months after procedure

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: Age between 18 and 75 years Symptomatic drug refractory (more than 2 antiarrhythmic drugs) paroxysmal or persistent AF Documentation of AF on 12 lead ECG and/ or Holter Left atrium of less than 55 mm Informed consent signed by the patient Exclusion Criteria: Previous Ablation or operation for AF Contra-indication for heart catheterisation Cardioversion for AF during the 2 weeks before the procedure
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Thomas Arentz, MD
Phone
004976334020
Email
thomas.arentz@herzzentrum.de
First Name & Middle Initial & Last Name or Official Title & Degree
Dietmar Trenk
Phone
004976334020
Email
dietmar.trenk@herzzentrum.de
Facility Information:
Facility Name
Herz-Zentrum
City
Bad Krozingen
ZIP/Postal Code
79189
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Thomas Arentz, MD
Phone
004976334020
Email
thomas.arentz@herzzentrum.de
First Name & Middle Initial & Last Name & Degree
Reinhold Weber, MD
Phone
004976334020
Email
reinhold.weber@herzzentrum.de

12. IPD Sharing Statement

Citations:
PubMed Identifier
24172190
Citation
Jesel L, Arentz T, Herrera-Siklody C, Trenk D, Zobairi F, Abbas M, Weber R, Minners J, Toti F, Morel O. Do atrial differences in endothelial damage, leukocyte and platelet activation, or tissue factor activity contribute to chamber-specific thrombogenic status in patients with atrial fibrillation? J Cardiovasc Electrophysiol. 2014 Mar;25(3):266-70. doi: 10.1111/jce.12312. Epub 2013 Nov 22.
Results Reference
derived
PubMed Identifier
21920484
Citation
Herrera Siklody C, Arentz T, Minners J, Jesel L, Stratz C, Valina CM, Weber R, Kalusche D, Toti F, Morel O, Trenk D. Cellular damage, platelet activation, and inflammatory response after pulmonary vein isolation: a randomized study comparing radiofrequency ablation with cryoablation. Heart Rhythm. 2012 Feb;9(2):189-96. doi: 10.1016/j.hrthm.2011.09.017. Epub 2011 Sep 13.
Results Reference
derived

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A Prospective Randomized Study Comparing Radiofrequency Energy With Cryoenergy

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