Ranolazine for the Prevention of Atrial Fibrillation After Electrical Cardioversion

PHASE3TerminatedINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

March 31, 2012

Primary Completion Date

June 30, 2014

Study Completion Date

June 30, 2014

Conditions
Atrial Fibrillation
Interventions
DRUG

Ranolazine

Patients will be started on ranolazine 500mg twice daily. The first dose will be administered the day of cardioversion. The dose will be doubled after 2 weeks to 1000mg twice daily as tolerated for a total of six months.

DRUG

Matching placebo

Patients will be started on a matching placebo twice daily. The first dose will be administered the day of cardioversion and continued for a total of six months.

Trial Locations (2)

73104

Oklahoma City VA Medical Center, Oklahoma City

OU Medical Center, Oklahoma City

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Gilead Sciences

INDUSTRY

lead

University of Oklahoma

OTHER