Microvention AnEurysm & STroke Real-life Data cOllection (MAESTRO-1)

MicroVention

Status: Enrolling

Conditions: Intracranial Aneurysm, Wide Neck Aneurysm, Large Neck Aneurysm Lesion; Aneurysmal Subarachnoid Hemorrhage; Intracranial Aneurysm

Treatments: Device: All Microvention Class III implantable device CE marked

Study type: Observational

Funder types: Industry

Identifiers

NCT06494436

MAESTRO-1

Details and patient eligibility

About

The MAESTRO-1 registry is a post-market, single-arm, non-interventional, multicenter registry

Full description

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

Enrollment: 750 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patient or legally authorized representative (LAR) is informed of the data collection and gives non-opposition or consent prior to the data collection in accordance with institutional and geographic requirements.
• Patient is treated for a ruptured or unruptured intracranial aneurysm using a commercially available MicroVention implant device as the primary treatment device and the decision to use this device has been made by the treating physician outside the context of the MAESTRO-1 study.

Exclusion criteria

• Patient is or is expected to be inaccessible for follow-up.
• Patient is participating or intends to participate in another study that changes the site practice.
• Patient has been previously enrolled into the MAESTRO-1 study.