Safety and Performance of the Neuroform Atlas™ Stent System
NCT04162483 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 310
Last updated 2020-06-17
Summary
The objective of this retrospective study is to describe in real-life settings the clinical practice, utilization and the treated population outcomes at 1-year (12-16 months) follow-up at selected, representative centers in France.
Conditions
- Intracranial Aneurysm
Interventions
- DEVICE
-
Neuroform Atlas Stent System
Stenting Assisted coiling procedure
Sponsors & Collaborators
-
Stryker Neurovascular
lead INDUSTRY
Principal Investigators
-
Emmanuel Houdart, MD · Hopital Lariboisière
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-11-19
- Primary Completion
- 2021-05-15
- Completion
- 2021-07-15
Countries
- France
Study Locations
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