CAPTURE 2 Post-Marketing Registry

CompletedOBSERVATIONAL
Enrollment

6,426

Participants

Timeline

Start Date

March 31, 2006

Primary Completion Date

March 31, 2010

Study Completion Date

May 31, 2010

Conditions
Carotid Artery Disease
Interventions
DEVICE

RX ACCULINK, RX ACCUNET Embolic Protection System

1\) To provide an ongoing post-market surveillance mechanism to document clinical outcomes. 2) To provide additional information that the RX ACCULINK™ and RX ACCUNET™ can be used safely by a wide range of physicians under commercial use conditions. 3) To evaluate the adequacy of Abbott Vascular's physician training program.

Trial Locations (1)

95054

Abbott Vascular, Santa Clara

Sponsors
All Listed Sponsors
lead

Abbott Medical Devices

INDUSTRY