Safety and Performance of the Neuroform Atlas™ Stent System

Last updated: June 16, 2020
Sponsor: Stryker Neurovascular
Overall Status: Active - Recruiting

Phase

N/A

Condition

Aneurysm

Treatment

N/A

Clinical Study ID

NCT04162483
T4062
  • All Genders

Study 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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patient who had undergone a stent assisted intracranial aneurysm coiling with Neuroform Atlas for the treatment of intracranial aneurysm(s) between 1st Feb 2017 and 1st March 2 018.

  • Patient and/or their representative have/has received the written information concerning the study and not expressed opposition to the collection of his data

Study Design

Total Participants: 310
Study Start date:
November 19, 2019
Estimated Completion Date:
July 15, 2021

Study 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.

Connect with a study center

  • CHU Gui de Chauliac

    Montpellier, F-34295
    France

    Active - Recruiting

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