186
Participants
Start Date
January 1, 2011
Primary Completion Date
January 31, 2015
Study Completion Date
July 31, 2016
No Amiodarone
This is a randomized study whereby patients who would routinely/usually be scheduled to receive Amiodarone as their anti-arrhythmic medication post surgical ablation will be randomly assigned to receive Amiodarone or no Amiodarone, but all other medications would remain as prescribed for patients following surgical ablation which will include beta blockade therapy unless contraindicated which is an American Heart Associated and Heart Rhythm Society recognized treatment.
Inova Fairfax Hospital, Falls Church
Lead Sponsor
Inova Health Care Services
OTHER