Trials / Completed
CompletedNCT03642639
A Study to Look at Performance of MICRUSFRAME and GALAXY Coils for the Treatment of Intracranial Aneurysms
A Prospective, Multi-center, Single Arm Study to Obtain "Real World" Clinical Data and Characterize the Acute and Long-term Performance of the MICRUSFRAME and GALAXY Coils Including the PulseRider Aneurysm Neck Reconstruction Device for the Endovascular Treatment of Intracranial Aneurysms
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 809 (actual)
- Sponsor
- Cerenovus, Part of DePuy Synthes Products, Inc. · Industry
- Sex
- All
- Age
- 21 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
A post-market registry evaluating ruptured/unruptured aneurysms treated with MICRUSFRAME and GALAXY coils
Detailed description
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
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | MICRUSFRAME and GALAXY coils | MICRUSFRAME and GALAXY Coils |
Timeline
- Start date
- 2018-08-23
- Primary completion
- 2025-06-12
- Completion
- 2025-06-12
- First posted
- 2018-08-22
- Last updated
- 2025-12-19
Locations
51 sites across 10 countries: United States, Belgium, France, Germany, Israel, Italy, Japan, Portugal, Spain, Switzerland
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03642639. Inclusion in this directory is not an endorsement.