For Healthcare Professionals

A Study to Look at Performance of MICRUSFRAME and GALAXY Coils for the Treatment of Intracranial Aneurysms

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About the study

A post-market registry evaluating ruptured/unruptured aneurysms treated with MICRUSFRAME and GALAXY coils
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria:

  1. Patient is between 21 and 80 years of age
  2. Patient has an intracranial saccular aneurysm, ruptured or unruptured, suitable for embolization with coils
  3. Patient is able and willing to comply with protocol and follow-up requirements

EXCLUSION CRITERIA

Exclusion Criteria:

  1. Pre-planned staged procedure on unruptured aneurysm
  2. More than one aneurysm requiring treatment during the course of study
  3. Fusiform aneurysm
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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.
Phone iconCall 9494668021Email iconEmail Study Center

Study’s details


Contition

Aneurysms

Age (in years)

21 - 80

Phase

Not Applicable

Participants needed

850

Est. Completion Date

Jun 30, 2026

Treatment type

Interventional


Sponsor

Cerenovus, Part of DePuy Synthes Products, Inc.

ClinicalTrials.gov identifier

NCT03642639

Study number

CNV_2017_01

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