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