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Clinical Trials/NCT06803615
NCT06803615
Active, not recruiting
Not Applicable

The Use of Beat-to-Beat Noninvasive 3D Mapping to Study Patients Candidates for Concomitant Surgical Ablation for Persistent and Long-standing Persistent Atrial Fibrillation

Medical University of Vienna1 site in 1 country51 target enrollmentStarted: January 13, 2017Last updated:

Overview

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
51
Locations
1
Primary Endpoint
The patients electrophysiological mapping results acquired with ECGI will be analyzed: Number and distribution of rotor and focal activities will be measured.

Overview

Brief Summary

The purpose of this study is to assess the electrophysiological mechanism of atrial fibrillation by means of a beat-to-beat noninvasive 3D mapping method in patients with concomitant persistent and long-standing persistent atrial fibrillation undergoing surgical ablation.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 90 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • legal age (18-90a)
  • life expectancy \> 2 years
  • patients suffering from persistent and long standing atrial fibrillation
  • scheduled for concomitant surgical ablation
  • possibility to follow-up
  • given informed consent

Exclusion Criteria

  • vulnerable patient groups
  • pregnancy
  • any previous surgical ablation
  • acute surgical indications
  • any physical condition that leads to a life expectancy of less than two years
  • any contraindication to the treatments necessary for the trial's conduction as e.g.
  • known allergic reaction to contrast agent
  • known allergic reaction to antiarrhythmic drugs
  • claustrophobia or anxiety in small spaces
  • severe renal impairment

Outcomes

Primary Outcomes

The patients electrophysiological mapping results acquired with ECGI will be analyzed: Number and distribution of rotor and focal activities will be measured.

Time Frame: Prior to the planned procedure.

The primary objective of this study is to measure the patients electrophysiological mapping results acquired with ECGI, namely the number and distribution of focal and rotor activities.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Emilio Osorio, MD

Principal Investigator

Medical University of Vienna

Study Sites (1)

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