Clinical trial
CORE: Study to Evaluate the Conducted AF-Response-Algorithm in Patients…
NCT00170313 · Medtronic Cardiac Rhythm and Heart Failure, Industry · Terminated
Key facts
| NCT number | NCT00170313 |
|---|---|
| Title | CORE: Study to Evaluate the Conducted AF-Response-Algorithm in Patients Suffering From Heart Failure and Atrial Fibrillation |
| Official title | Conducted AF-Response Study (Study to Evaluate the Conducted AF-Response-Algorithm in Patients Suffering From Heart Failure and Atrial Fibrillation Treated With InSync III Marquis) |
| Lead sponsor | Medtronic Cardiac Rhythm and Heart Failure, Industry |
| Collaborators | Medtronic Industry |
| Status | Terminated |
| Phase | Phase 4 |
| Study type | Interventional |
| Conditions | Heart Failure, Sudden Cardiac Death, Atrial Fibrillation |
| Intervention type | Device |
| Interventions | Conducted AF-Response Algorithm (CAFR) On, Conducted AF-Response Algorithm (CAFR) Off |
| Enrollment | 100 |
| Start date | Dec 1, 2003 |
| Completion | Jan 1, 2007 |
| First posted | Sep 15, 2005 |
| Last update posted | Jul 3, 2025 |
| Countries | Germany |
At a glance
- 1–9 Study sites
- No Results posted
- 1–9 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: