NCT01930071

PQ Bypass Guide Wire Delivery System for Femoropopliteal Bypass

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 4 (actual)
• Sponsor: Endologix · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

To assess the safety of performing a percutaneous fem-pop bypass using the PQ Bypass Guidewire Delivery System and commercially available stent grafts.

Detailed description

Multi-center, single-arm first-in-man study utilizing the PQ Bypass Guide Wire Delivery System to access, deliver guidewires and implant stent grafts for a percutaneous femoropopliteal (fem-pop) bypass.

Conditions

• Peripheral Arterial Disease

Interventions

Type	Name	Description
DEVICE	PQ Bypass Guide Wire Delivery System	The PQ Bypass Guide Wire Delivery System is used to bypass lesions in the peripheral vasculature percutaneously. A guidewire is placed from the artery proximal to the lesion to the artery distal to the lesion using the vein as a conduit with the Guidewire Delivery System. Once in place, commercially available stent grafts will be placed to complete the bypass.

Timeline

• Start date: 2013-11-01
• Primary completion: 2015-06-01
• Completion: 2015-06-01
• First posted: 2013-08-28
• Last updated: 2024-03-01

Locations

1 site across 1 country: New Zealand