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International Retrospective Study of Pipeline Embolization Device

NCT01558102 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 793

Last updated 2024-10-08

No results posted yet for this study

Summary

The primary objective of this retrospective study is to determine the incidence of important safety outcomes in patients who have undergone Pipeline Embolization Device placement for intracranial aneurysms (IAs). This study does not effect patient care, simply it is designed to observe and capture information from numerous hospitals.

Data collection will be initiated starting March 2012 and continue until approximately April 2017.

Conditions

  • Brain Aneurysms

Sponsors & Collaborators

  • Medtronic Neurovascular Clinical Affairs

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-03-31
Primary Completion
2013-07-31
Completion
2013-07-31

Countries

  • United States
  • Argentina
  • Canada
  • France
  • Hungary
  • Italy

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 NCT01558102 on ClinicalTrials.gov