Clinical Research Details

Descriptive Information
Double sequence external defibrillation: A randomized controlled trial in patients with atrial fibrillation refractory to DC cardioversion

Gilbert Abou Dagher
ga66@aub.edu.lb

BIO-2017-0457
Ongoing

Clinical Research - Therapeutic interventions  

Phase 3  

No
Collaborators
  • Marwan Refaat
  • Hani Tamim
  • Bernard Abi Saleh
  • Maurice Khoury
  • Iskandar Berbari
  • Rawan Safa
  • Mohammad Sabra
Coordinators
Iskandar Berbari
ib24@aub.edu.lb
Extension: 7066
Rawan Safa
rs212@aub.edu.lb
Extension: 7875
Conditions and Keywords
Refractory Atrial Fibrillation,DSED,CCU
Double sequential electrical defibrillation,DSED,Atrial Fibrillation,Refractory Atrial Fibrillation,Cardioversion
Study Design
Treatment
Prospective
Parallel
Randomized
Case Control
Eligibility and IRB
Both
Min: 18
Max:
Yes
No

This study is a Phase III, randomized controlled, superiority trial, with two parallel groups, conducted in one academic medical center.  

The objective of this study is to assess the effectiveness of double sequence defibrillation in reverting patients with Atrial Fibrillation (AF) refractory to two trials of direct current cardioversion.

We hypothesize that in patients with AF refractory to 2 or more trials of Direct Current (DC) cardioversion, the use of double sequential defibrillation (DSED) has a higher success rate in terms of reverting patients to sinus rhythm as compared to an additional trial of DC cardioversion.


All AF patients admitted to the CCU for DC cardioversion, and refractory to at least two trials of DC cardioversion will be eligible for this study


Patients presenting to the CCU with persistent AFfor 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.  


All AF patients admitted to the CCU for DC cardioversion, and refractory to at least two trials of DC cardioversion will be eligible for this study.

Excluded from this study will be patients with AF not requiring DC cardioversion, or those with AF who reverted after a maximum of two trials of DC cardioversion.