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

  • End date
    Jun 30, 2026
  • participants needed
  • sponsor
    Cerenovus, Part of DePuy Synthes Products, Inc.
Updated on 18 September 2023
ruptured aneurysm
intracranial aneurysm
embolization procedure


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


A registry to collect real world data on the use of Cerenovus coils. The study will be a post-market registry evaluating ruptured/unruptured aneurysms treated with MICRUSFRAME and GALAXY coils

Condition Aneurysms
Treatment Spectra Micrusframe and Spectra Galaxy coils, MICRUSFRAME and GALAXY coils
Clinical Study IdentifierNCT03642639
SponsorCerenovus, Part of DePuy Synthes Products, Inc.
Last Modified on18 September 2023


Yes No Not Sure

Inclusion Criteria

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

Exclusion Criteria

Pre-planned staged procedure on unruptured aneurysm
More than one aneurysm requiring treatment during the course of study
Fusiform aneurysm
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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