Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT02309203

Canadian Study of the MicroVention Flow Re-Direction (FRED) Endoluminal Device Stent System in the Treatment of Intracranial Aneurysms

Canadian Study of the MicroVention Flow Re-Direction (FRED) Endoluminal Device Stent System in the Treatment of Intracranial Aneurysms - The CanFRED Trial

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Centre hospitalier de l'Université de Montréal (CHUM) · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The study objective is to evaluate the safety and effectiveness of the MicroVention FRED System when used in the treatment of wide-necked intracranial aneurysms.

Conditions

Interventions

TypeNameDescription
DEVICEFREDFlow Re-Direction Endoluminal Device

Timeline

Primary completion
2017-02-01
Completion
2017-09-01
First posted
2014-12-05
Last updated
2015-07-28

Source: ClinicalTrials.gov record NCT02309203. Inclusion in this directory is not an endorsement.

Canadian Study of the MicroVention Flow Re-Direction (FRED) Endoluminal Device Stent System in the Treatment of Intracra (NCT02309203) · Clinical Trials Directory