Double Sequential External Defibrillation in Patients With Atrial Fibrillation Refractory to DC Cardioversion

Sponsor
American University of Beirut Medical Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT03827915
Collaborator
(none)
100
1
2
60
1.7

Study Details

Study Description

Brief Summary

Atrial fibrillation (AF) is a common cardiac arrhythmia that leads to increased risk of heart failure, hospitalization, thromboembolic events, and death. Restoration of normal heart rhythm is performed in many patients with AF to improve symptoms. In this study, the investigators will consider patients who fail 2 or more trials of DC cardioversion as having refractory AF.

The aim of this study is to assess whether the use of double sequential defibrillation in patients with refractory AF has a higher success rate in reverting them to a normal heart rhythm than a third cardioversion.

This is a phase III, randomized controlled, single-centered, superiority trial. All patients with AF admitted to the coronary care unit (CCU) for DC cardioversion, and refractory to at least two trials of DC cardioversion will be enrolled. Patients are randomized into two arms: the first will receive a third trial of DC cardioversion (standard of care) and the second will receive double sequential external defibrillation.

The resolution of AF by reverting back to normal sinus rhythm is the primary outcome of the investigators. This will be determined using EKG (electrocardiogram) immediately after DC cardioversion or double sequential defibrillation.

Condition or Disease Intervention/Treatment Phase
  • Device: Double sequential external defibrillation
N/A

Detailed Description

Patients presenting to the CCU with persistent AF for direct current (DC) cardioversion, who meet the inclusion criteria and fail to revert to normal sinus rhythm after two DC cardioversion attempts will be invited for enrollment in the study. No sampling will be carried out for the sake of this study.

Patients meeting the eligibility criteria will receive double sequential external defibrillation (DSED) or a third DC cardioversion (standard of care).

DSED is the process of using two defibrillators near simultaneously at their highest allowed energy setting and aims to treat refractory atrial fibrillation. The first set of pads is placed in the traditional anterolateral position and the second set can be either placed adjacent to the first set (antero-lateral) or in the antero-posterior position. Shocks are then delivered simultaneously or near simultaneously.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Phase III, randomized controlled, superiority trial, with two parallel groups, conducted in one academic medical centerPhase III, randomized controlled, superiority trial, with two parallel groups, conducted in one academic medical center
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Double Sequence External Defibrillation: A Randomized Controlled Trial in Patients With Atrial Fibrillation Refractory to DC Cardioversion
Actual Study Start Date :
Jan 21, 2019
Anticipated Primary Completion Date :
Jan 21, 2024
Anticipated Study Completion Date :
Jan 21, 2024

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Third trial of DC cardioversion

Patients with atrial fibrillation who fail to revert to sinus rhythm after two failed DC cardioversion attempts will receive a third trial of DC cardioversion (Standard of care)

Experimental: Double sequential external defibrillation

Patients with atrial fibrillation who fail to revert to sinus rhythm after two failed DC cardioversion attempts will receive DSED

Device: Double sequential external defibrillation
DSED is the process of using two defibrillators near simultaneously at their highest allowed energy setting and aims to treat refractory atrial fibrillation. The first set of pads is placed in the traditional anterolateral position and the second set can be either placed adjacent to the first set (antero-lateral) or in the antero-posterior position. Shocks are then delivered simultaneously or near simultaneously

Outcome Measures

Primary Outcome Measures

  1. Number of participants with atrial fibrillation who revert back to normal sinus rhythm using Double Sequential External Defibrillation after two failed attempts of DC cardioversion. [15 minutes]

    Number of participants with atrial fibrillation who revert back to normal sinus rhythm using Double Sequential External Defibrillation after two failed attempts of DC cardioversion . This will be determined using an EKG (Electrocardiogram) immediately after double sequential external defibrillation.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Atrial Fibrillation patients admitted to the CCU for DC cardioversion, and refractory to at least two trials of DC cardioversion
Exclusion Criteria:
  • Patients with Atrial Fibrillation not requiring DC cardioversion

  • Patients with Atrial Fibrillation who reverted after a maximum of two trials of DC cardioversion

Contacts and Locations

Locations

Site City State Country Postal Code
1 American University of Beirut Medical Center Beirut Lebanon

Sponsors and Collaborators

  • American University of Beirut Medical Center

Investigators

  • Principal Investigator: Gilbert Abou Dagher, M.D., American University of Beirut Medical Center

Study Documents (Full-Text)

More Information

Publications

Responsible Party:
American University of Beirut Medical Center
ClinicalTrials.gov Identifier:
NCT03827915
Other Study ID Numbers:
  • BIO-2017-0457
First Posted:
Feb 4, 2019
Last Update Posted:
Feb 4, 2019
Last Verified:
Jan 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by American University of Beirut Medical Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 4, 2019