Safety and Performance of the Neuroform Atlas™ Stent System

NCT04162483 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 310

Last updated 2020-06-17

No results posted yet for this 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.

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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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04162483 on ClinicalTrials.gov