Trials / Unknown
UnknownNCT04162483
Safety and Performance of the Neuroform Atlas™ Stent System
Safety and Performance of the Neuroform Atlas™ Stent System in Patients Requiring Stent Assisted Intracranial Aneurysm Treatment in France - A National, Retrospective Multi-center Registry
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 310 (estimated)
- Sponsor
- Stryker Neurovascular · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
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.
Detailed description
This proposed ATLAS FR study will be a retrospective review conducted to expand our knowledge of the clinical outcomes in subjects treated in France between 01 February 2017 and 01 March 2018. This will provide a comprehensive data set that is specifically representative of the Atlas stent use in France.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Neuroform Atlas Stent System | Stenting Assisted coiling procedure |
Timeline
- Start date
- 2019-11-19
- Primary completion
- 2021-05-15
- Completion
- 2021-07-15
- First posted
- 2019-11-14
- Last updated
- 2020-06-17
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT04162483. Inclusion in this directory is not an endorsement.