Clinical trial
REPLACE: Implantable Cardiac Pulse Generator Replacement Registry
NCT00395447 · Biotronik, Inc., Industry · Completed
Key facts
| NCT number | NCT00395447 |
|---|---|
| Title | REPLACE: Implantable Cardiac Pulse Generator Replacement Registry |
| Official title | Prospective Assessment of the Complication Rate After Device Replacement Due to ERI, Advisory or Upgrade |
| Acronym | REPLACE |
| Lead sponsor | Biotronik, Inc., Industry |
| Status | Completed |
| Study type | Observational |
| Conditions | Device Replacement, Elective Replacement (ERI), Device Advisory, Device Upgrade, Postoperative Complications |
| Intervention type | Procedure |
| Interventions | Straight-forward Device Replacement, Device Replacement with Upgrade |
| Enrollment | 1,744 |
| Start date | Jul 1, 2007 |
| Primary completion | Jun 1, 2009 |
| Completion | Jun 1, 2009 |
| First posted | Nov 3, 2006 |
| Last update posted | Apr 14, 2015 |
| Countries | United States |
At a glance
- 10–99 Study sites
- Yes 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: