Clinical trial
High Intensity Focused Ultrasound (HIFU) Ablation System Study
NCT00392106 · ProRhythm, Inc., Industry · Suspended
Key facts
| NCT number | NCT00392106 |
|---|---|
| Title | High Intensity Focused Ultrasound (HIFU) Ablation System Study |
| Official title | Study of Focused Circumferential UltraSound for the Treatment of Atrial Fibrillation |
| Lead sponsor | ProRhythm, Inc., Industry |
| Status | Suspended |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Atrial Fibrillation |
| Intervention type | Device, Drug |
| Interventions | propafenone, flecainide, dofetilide, sotolol, Pulmonary vein ablation, Amiodarone |
| Enrollment | 240 |
| Start date | Apr 1, 2006 |
| Primary completion | Dec 1, 2010 |
| Completion | Jun 1, 2011 |
| First posted | Oct 25, 2006 |
| Last update posted | Jun 17, 2008 |
| Countries | Czechia, United States |
At a glance
- 10–99 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: