ONYX Evaluation in the Endovascular Treatment of Intracranial Dural Arteriovenous Fistulae

NCT02180945 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 110

Last updated 2019-01-28

No results posted yet for this study

Summary

The objective of this study is to evaluate the safety and performance post last embolization with Onyx

Conditions

  • Arteriovenous Fistula

Sponsors & Collaborators

  • Medtronic Neurovascular Clinical Affairs

    lead INDUSTRY

Principal Investigators

  • Christophe Cognard, Prof. Dr. · University Hospital, Toulouse

  • Frédéric Ricolfi, Prof. Dr. · Centre Hospitalier Universitaire Dijon

  • Patrick Courthéoux, Prof. Dr. · University Hospital, Caen

  • Laurent Spelle, Prof. Dr. · Hôpital Beaujon

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-07-31
Primary Completion
2016-05-31
Completion
2016-05-31

Countries

  • France

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 NCT02180945 on ClinicalTrials.gov