NCT00349908

A Feasibility Study of the Cordis Neurovascular Self Expanding Stent System in Intracranial Arteries

• Status: Completed
• Phase: Phase 1
• Study type: Interventional
• Enrollment: 20 (actual)
• Sponsor: Codman & Shurtleff · Industry
• Sex: All
• Age: 18 Years – 80 Years
• Healthy volunteers: Not accepted

Summary

Feasibility study to assess safety of treating patients with self expanding stent in intracranial arteries.

Detailed description

Feasibility study to assess safety of treating patients with self expanding stent in intracranial arteries. Patients will be followed for 6 months with assessments related to technical feasibility and adverse events.

Conditions

• Atherosclerosis
• Aneurysm

Interventions

Type	Name	Description
DEVICE	Cordis Neurovascular ENTERPRISE Self Expanding Stent System	Implantation of the device ENTERPRISE used to treat symptomatic stenosis in intracranial arteries.
DEVICE	Cordis Neurovascular ENTERPRISE Self Expanding Stent System	Implantation of the device ENTERPRISE to treat wide-necked aneurysms

Timeline

• Start date: 2006-09-01
• Primary completion: 2008-10-01
• Completion: 2009-03-01
• First posted: 2006-07-10
• Last updated: 2014-06-30
• Results posted: 2013-10-11

Locations

1 site across 1 country: Argentina