The MAESTRO registry is a post-market, single-arm, non-interventional, multicenter registry
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.
Study Type
OBSERVATIONAL
Enrollment
1,000
Endovascular treatment of ruptured or unruptured intracranial aneurysms with commercially available MicroVention implant devices.
Endovascular treatment of acute ischemic stroke with commercially available MicroVention devices.
Álvaro Cunqueiro Hospital - University Hospital Complex of Vigo, Department of Radiology
Vigo, Pontevedra, Spain
RECRUITINGCohort 1: Proportion of aneurysms with complete occlusion
based on Raymond-Roy occlusion classification (RROC) evaluated by an independent Core laboratory
Time frame: 18 (±6) months
Cohort 2: Proportion of patients achieving final mTICI ≥ 2b revascularization
based on independent Corelab assessment
Time frame: Mechanical trombectomy Procedure
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.