NCT00349570

Xtract™ Aspiration Catheter Registry Study

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: —
• Sponsor: Lumen Biomedical · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

Intra-coronary thrombosis and thromboembolism continues to be a challenge for percutaneous coronary and other vascular interventional techniques. The Xtract™ Aspiration Catheter is a single use device designed to remove fresh, soft emboli and thrombi from the arterial system using standard catheter techniques, compatible with 6 Fr guide catheters and 0.014 guidewires. The purpose of this registry study is to validate the design and demonstrate the performance of the Xtract Aspiration Catheter as a thrombectomy catheter during percutaneous intervention of vessels in the arterial system. Subjects will be enrolled during percutaneous intervention when the Interventional Physician decides a thrombectomy catheter is needed to remove thrombus during the procedure.

Conditions

• Fresh Soft Emboli or Thrombi in the Arteries.

Interventions

Type	Name	Description
DEVICE	Xtract Aspiration Catheter

Timeline

• Start date: 2006-08-01
• Completion: 2008-03-01
• First posted: 2006-07-07
• Last updated: 2008-10-21

Locations

2 sites across 1 country: New Zealand