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Neurovascular Embolization Cover for Treatment of Intracranial Aneurysms and Carotid/Vertebrobasilar Fistulae

NCT01054391 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2010-01-22

No results posted yet for this study

Summary

The purpose of this study is to determine whether the NEC device can effectively occlude the intracranial aneurysm or the carotid/vertebrobasilar fistula and maintain parent vessel patency

Conditions

  • Intracranial Aneurysms
  • Cavernous Carotid Fistula
  • Vertebrobasilar Fistula

Interventions

DEVICE

NEC - Neurovascular Embolization Cover

Implantation of NEC for the treatment of intracranial aneurysms and carotid/vertebrobasilar fistuale arising from a parent vessel of 2.5 to 4.5mm

Sponsors & Collaborators

  • Nfocus Neuromedical

    lead INDUSTRY

Principal Investigators

  • Olav Jansen, Prof. Dr. med. · Universitatsklinikum Schleswig-Holstein Campus Kiel Institut fur Neuroradiologie

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
19 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-10-31
Primary Completion
2010-12-31

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01054391 on ClinicalTrials.gov