Complex Aneurysm Registry - Real-World Evidence Data Collection Intracranial Aneurysm Treatment Devices

NCT06215105 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 750

Last updated 2025-10-01

No results posted yet for this study

Summary

To collect real-world evidence allowing assessment of functional, imaging, and safety outcomes of commercially available MicroVention devices used for the endovascular treatment of intracranial aneurysms (IA) at the direction of the treating physician.

Conditions

  • Aneurysm Cerebral

Interventions

DEVICE

Intracranial Aneurysm Devices

Intracranial Aneurysm occlusion

Sponsors & Collaborators

  • Microvention-Terumo, Inc.

    lead INDUSTRY

Principal Investigators

  • TBD TBD

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-01-08
Primary Completion
2029-01-08
Completion
2029-01-08
FDA Device
Yes

Countries

  • United States

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 NCT06215105 on ClinicalTrials.gov