Solitaire Aneurysm Remodeling Registry

NCT04905303 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2021-05-27

No results posted yet for this study

Summary

The objective of the registry is to evaluate the effectiveness and performance of the Solitaire Neurovascular Remodeling Device when used with embolic coils in the treatment of intracranial aneurysms.

Conditions

  • Intracranial Saccular Aneurysm, Either Rupture or Unruptured
  • Wide Neck Aneurysm

Sponsors & Collaborators

  • Medtronic Neurovascular Clinical Affairs

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-02-28
Primary Completion
2011-02-28
Completion
2011-06-30

Countries

  • France

Study Locations

More Related Trials

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 NCT04905303 on ClinicalTrials.gov