Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06494436

Microvention AnEurysm & STroke Real-life Data cOllection

Microvention Aneurysm & Stroke Real-life Data Collection

Status
Recruiting
Phase
Study type
Observational
Enrollment
1,000 (estimated)
Sponsor
Microvention-Terumo, Inc. · Industry
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The MAESTRO registry is a post-market, single-arm, non-interventional, multicenter registry

Detailed description

Electronic platform to collect real-world clinical data, evaluate and periodically report safety and effectiveness of CE approved and commercially available Microvention devices used for the endovascular treatment of Intracranial aneurysms and acute ischemic stroke.

Conditions

Interventions

TypeNameDescription
DEVICEAll Microvention Class III implantable device CE markedEndovascular treatment of ruptured or unruptured intracranial aneurysms with commercially available MicroVention implant devices.
DEVICEAll Microvention Mechanical Thrombectomy Class III device CE markedEndovascular treatment of acute ischemic stroke with commercially available MicroVention devices.

Timeline

Start date
2024-12-30
Primary completion
2029-12-30
Completion
2030-06-30
First posted
2024-07-10
Last updated
2026-02-09

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT06494436. Inclusion in this directory is not an endorsement.