drugset / Trial / NCT00267930
Study of RSD1235-SR for the Prevention of Atrial Fibrillation/Atrial Flutter Recurrence
RandomizedParallel-groupQuadruple-blindPrevention
Summary
This study is designed to evaluate the safety, tolerability and preliminary efficacy of vernakalant (oral) in subjects with sustained atrial fibrillation of greater than 72 hours and less than 6 months duration
Timeline
- Start
- 2005-12
- Primary completion
- —
- Completion
- 2006-08
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Vernakalant | Other / unclassified | 300 mg | Oral |
| Subject | Vernakalant | Other / unclassified | 600 mg | Oral |