Aneurysm Study of Pipeline in an Observational Registry

NCT01557036 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2015-01-21

No results posted yet for this study

Summary

The primary objective of this study is to further expand the body of clinical knowledge in patients undergoing Pipeline Embolization Device (Pipeline or PED) placement for intracranial aneurysms (IAs or ICAs) according to Pipeline's labeled indication.

Conditions

  • Brain Aneurysm

Interventions

DEVICE

Pipeline Embolization Device

Aneurysms treated independent of study entry with the Pipeline Embolization Device. This is an observational, non-interventional study.

Sponsors & Collaborators

  • Medtronic Neurovascular Clinical Affairs

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-05-31
Primary Completion
2014-05-31

Countries

  • United States
  • Argentina
  • Belgium
  • Canada
  • France
  • Germany
  • Italy
  • Switzerland

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 NCT01557036 on ClinicalTrials.gov