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Electrophysiologically Guided PAcing Site Selection Study (EPASS)

Primary Purpose

Sinus Arrhythmia, Atrial Fibrillation

Status
Completed
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
IAS pacing - study group
IAS pacing control group
Pacing RAA study group
Pacing RAA control group
Sponsored by
Medtronic BRC
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Sinus Arrhythmia focused on measuring atrial fibrillation, interatrial septum, atrial pacing, symptomatic sinus node dysfunction,, pacemaker indication class I

Eligibility Criteria

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

Inclusion Criteria: Symptomatic sinus node dysfunction More than 18 years old Signed informed consent Exclusion Criteria: Less than 18 years old Pregnancy Anamnestic transient ischemic attack (TIA) or stroke Neoplastic or any other severe disease reducing life expectancy Heart surgery in the last 3 months Left atrial diameter > 55mm, determined in the parasternal long-axis view (during either sinus rhythm or atrial fibrillation) Participation in other studies

Sites / Locations

  • Azienda Ospedaliera di Desenzano del Garda
  • Divisione di Cardiologia
  • Divisione di Cardiologia - CRN
  • Divisione di Cardiologia - Ospedale Cisanello
  • Divisione di Cardiologia - Ospedale San Pietro Igneo
  • Divisione di Cardiologia - Ospedale Molinette
  • Divisione di Cardiologia - Ospedale Civile ULSS 13
  • Divisione di Cardiologia - Presidi Ospedalieri Riuniti

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Active Comparator

Active Comparator

Arm Label

1. IAS pacing - study group

2. IAS pacing-control group

3. RAA Pacing - study group

4. RAA Pacing - control group

Arm Description

Patients were first submitted to electrophysiological study to assess Delta CTos > or < 50 ms. Then they were randomized to interatrial septum pacing od right atrial appendage. This arm (1) includes patients with Delta CTos >50 ms and randomized IAS pacing. IAS Pacing -Study Group: Patients with Delta CTos >50 ms (study group) at the electrophysiologic study and randomized Interatrial Septum Pacing

(Delta CTos<50ms) Patients were first submitted to electrophysiological study to assess Delta CTos > or < 50 ms. Then they were randomized to interatrial septum pacing od right atrial appendage. This arm (2) includes patients with Delta CTos <50 ms and randomized IAS pacing. IAS Pacing -Control Group: Patients with Delta CTos <50 ms (control group) at the electrophysiologic study and randomized Interatrial Septum Pacing

Patients were first submitted to electrophysiological study to assess Delta CTos > or < 50 ms. Then they were randomized to interatrial septum pacing od right atrial appendage. This arm (3) includes patients with Delta CTos >50 ms and randomized Right Atrial Appendage pacing. RAA Pacing -Study Group: Patients with Delta CTos >50 ms (study group) at the electrophysiologic study and randomized Right Atrial Appendage pacing

Patients were first submitted to electrophysiological study to assess Delta CTos > or < 50 ms. Then they were randomized to interatrial septum pacing od right atrial appendage. This arm (4) includes patients with Delta CTos <50 ms and randomized Right Atrial Appendage pacing. RAA Pacing -Control Group: Patients with Delta CTos <50 ms (control group) at the electrophysiologic study and randomized Right Atrial Appendage pacing

Outcomes

Primary Outcome Measures

Number of Patients With Persistent Atrial Fibrillation (AF) After a Mean Follow-up of 15±7 Months: Comparison Between IAS and RAA Pacing in the Study Group
Persistent Atrial Fibrillation (AF) incidence

Secondary Outcome Measures

Number of Persistent Atrial Fibrillation (AF) Episodes: Comparison Between All Groups
Number of Patients With Permanent Atrial Fibrillation (AF)
Symptom Scale Questionnaire: Comparison Between All Groups
Number of Cardioversion: Comparison Between All Groups
Heart Failure: Comparison Between All Groups
Time to First Persistent Episode of Atrial Fibrillation (AF)
Number of Episodes/Day
AF Burden
Ventricular Pacing Percentage

Full Information

First Posted
October 13, 2005
Last Updated
September 20, 2013
Sponsor
Medtronic BRC
Collaborators
Medtronic
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1. Study Identification

Unique Protocol Identification Number
NCT00239226
Brief Title
Electrophysiologically Guided PAcing Site Selection Study
Acronym
EPASS
Official Title
Investigational New Drug Application/ Investigational Device Exemption Information
Study Type
Interventional

2. Study Status

Record Verification Date
April 2012
Overall Recruitment Status
Completed
Study Start Date
November 2005 (undefined)
Primary Completion Date
December 2008 (Actual)
Study Completion Date
March 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Medtronic BRC
Collaborators
Medtronic

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study is a long-term, prospective, and controlled evaluation of the incidence of persistent atrial fibrillation (AF) in patients with severe intra-right atrial conduction delay paced with preventive algorithms at the interatrial septum (IAS) versus right atrial appendage (RAA).
Detailed Description
The EPASS is a multicenter, prospective, randomized, and controlled study. Prior to entering the study, the patient should be informed and provide a written consent. In addition, the patient should meet all selection criteria. The Investigator has to check that all selection criteria are satisfied. Then the patient undergoes pacemaker implantation, receiving a pacemaker model T70 or Selection 9000 (or later version). Patients eligible for the study are enrolled and submitted to the evaluation of intra-light atrial conduction delay before device implantation. Besides, they are assigned to the group with severe RA conduction delay or with normal conduction delay. The randomization of the pacing site for both groups depends on the value of right atrial conduction delay, together with the associated diseases of the patients, sex and age. After implantation, a stabilization phase of 3-5 weeks is required to stabilize the leads: during this period the physician can optimize the device parameters. Neither the data regarding AF episodes nor cardioversion are collected. At the end of the stabilization phase the patient undergoes the 1st study follow-up and starts the monitoring period lasting 2 years. Regular follow-ups and data collection are scheduled every 6 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sinus Arrhythmia, Atrial Fibrillation
Keywords
atrial fibrillation, interatrial septum, atrial pacing, symptomatic sinus node dysfunction,, pacemaker indication class I

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
102 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1. IAS pacing - study group
Arm Type
Experimental
Arm Description
Patients were first submitted to electrophysiological study to assess Delta CTos > or < 50 ms. Then they were randomized to interatrial septum pacing od right atrial appendage. This arm (1) includes patients with Delta CTos >50 ms and randomized IAS pacing. IAS Pacing -Study Group: Patients with Delta CTos >50 ms (study group) at the electrophysiologic study and randomized Interatrial Septum Pacing
Arm Title
2. IAS pacing-control group
Arm Type
Experimental
Arm Description
(Delta CTos<50ms) Patients were first submitted to electrophysiological study to assess Delta CTos > or < 50 ms. Then they were randomized to interatrial septum pacing od right atrial appendage. This arm (2) includes patients with Delta CTos <50 ms and randomized IAS pacing. IAS Pacing -Control Group: Patients with Delta CTos <50 ms (control group) at the electrophysiologic study and randomized Interatrial Septum Pacing
Arm Title
3. RAA Pacing - study group
Arm Type
Active Comparator
Arm Description
Patients were first submitted to electrophysiological study to assess Delta CTos > or < 50 ms. Then they were randomized to interatrial septum pacing od right atrial appendage. This arm (3) includes patients with Delta CTos >50 ms and randomized Right Atrial Appendage pacing. RAA Pacing -Study Group: Patients with Delta CTos >50 ms (study group) at the electrophysiologic study and randomized Right Atrial Appendage pacing
Arm Title
4. RAA Pacing - control group
Arm Type
Active Comparator
Arm Description
Patients were first submitted to electrophysiological study to assess Delta CTos > or < 50 ms. Then they were randomized to interatrial septum pacing od right atrial appendage. This arm (4) includes patients with Delta CTos <50 ms and randomized Right Atrial Appendage pacing. RAA Pacing -Control Group: Patients with Delta CTos <50 ms (control group) at the electrophysiologic study and randomized Right Atrial Appendage pacing
Intervention Type
Procedure
Intervention Name(s)
IAS pacing - study group
Intervention Description
site of implant and permanent pacing
Intervention Type
Procedure
Intervention Name(s)
IAS pacing control group
Intervention Description
site of implant and permanent pacing
Intervention Type
Procedure
Intervention Name(s)
Pacing RAA study group
Intervention Description
site of implant and permanent pacing
Intervention Type
Procedure
Intervention Name(s)
Pacing RAA control group
Intervention Description
site of implant and permanent pacing
Primary Outcome Measure Information:
Title
Number of Patients With Persistent Atrial Fibrillation (AF) After a Mean Follow-up of 15±7 Months: Comparison Between IAS and RAA Pacing in the Study Group
Description
Persistent Atrial Fibrillation (AF) incidence
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Number of Persistent Atrial Fibrillation (AF) Episodes: Comparison Between All Groups
Time Frame
January 2009
Title
Number of Patients With Permanent Atrial Fibrillation (AF)
Time Frame
January 2009
Title
Symptom Scale Questionnaire: Comparison Between All Groups
Time Frame
January 2009
Title
Number of Cardioversion: Comparison Between All Groups
Time Frame
January 2009
Title
Heart Failure: Comparison Between All Groups
Time Frame
January 2009
Title
Time to First Persistent Episode of Atrial Fibrillation (AF)
Time Frame
January 2009
Title
Number of Episodes/Day
Time Frame
January 2009
Title
AF Burden
Time Frame
January 2009
Title
Ventricular Pacing Percentage
Time Frame
January 2009

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Symptomatic sinus node dysfunction More than 18 years old Signed informed consent Exclusion Criteria: Less than 18 years old Pregnancy Anamnestic transient ischemic attack (TIA) or stroke Neoplastic or any other severe disease reducing life expectancy Heart surgery in the last 3 months Left atrial diameter > 55mm, determined in the parasternal long-axis view (during either sinus rhythm or atrial fibrillation) Participation in other studies
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Giorgio Corbucci, PhD
Organizational Affiliation
Medtronic
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Roberto Verlato, MD
Organizational Affiliation
Camposampiero Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Azienda Ospedaliera di Desenzano del Garda
City
Desenzano
State/Province
BS
Country
Italy
Facility Name
Divisione di Cardiologia
City
Como
State/Province
CO
ZIP/Postal Code
22100
Country
Italy
Facility Name
Divisione di Cardiologia - CRN
City
Pisa
State/Province
PI
ZIP/Postal Code
56127
Country
Italy
Facility Name
Divisione di Cardiologia - Ospedale Cisanello
City
Pisa
State/Province
PI
ZIP/Postal Code
56127
Country
Italy
Facility Name
Divisione di Cardiologia - Ospedale San Pietro Igneo
City
Fucecchio
State/Province
Prato
Country
Italy
Facility Name
Divisione di Cardiologia - Ospedale Molinette
City
Torino
State/Province
TO
ZIP/Postal Code
10126
Country
Italy
Facility Name
Divisione di Cardiologia - Ospedale Civile ULSS 13
City
Mirano
State/Province
VE
ZIP/Postal Code
30035
Country
Italy
Facility Name
Divisione di Cardiologia - Presidi Ospedalieri Riuniti
City
Borgomanero
ZIP/Postal Code
28100
Country
Italy

12. IPD Sharing Statement

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Electrophysiologically Guided PAcing Site Selection Study

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