Clinical trial
Post-Approval Study of the Guidant Carotid Stent Systems and Embolic Protection…
NCT00180492 · Abbott Medical Devices, Industry · Completed
Key facts
| NCT number | NCT00180492 |
|---|---|
| Title | Post-Approval Study of the Guidant Carotid Stent Systems and Embolic Protection Systems: CAPTURE |
| Official title | Carotid RX ACCULINK(TM)/ACCUNET(TM) Post-Approval Trial to Uncover Unanticipated or Rare Events - CAPTURE |
| Lead sponsor | Abbott Medical Devices, Industry |
| Collaborators | Guidant Corporation Industry |
| Status | Completed |
| Study type | Interventional |
| Conditions | Atherosclerotic Disease, Carotid |
| Intervention type | Device |
| Interventions | RX ACCULINK(TM) Carotid Stent System and RX ACCUNET(TM) Embolic Protection System |
| Enrollment | 1,500 |
| Start date | Oct 1, 2004 |
| Primary completion | Dec 1, 2006 |
| Completion | Aug 1, 2007 |
| First posted | Sep 16, 2005 |
| Last update posted | Oct 29, 2008 |
| Countries | United States |
At a glance
- 1–9 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: