Status: Recruiting
Post Market Registry Study of Intracranial Aneurysms Treated With Sugita Clipping Devices
The objective of this study is to verify the performance and safety of the Sugita Aneurysm Clips devices when used as intended and to identify possible risk factors. Data collected will be used to support the continuing performance and safety of the devices in the post-market use environment in Europe. Subjects who have an intracranial aneurysm that the physician intends to treat with the subject devices will be included in the study. Subjects will be followup as per hospital standard of care for 5 years.
Participants needed: 150
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Mizuho CorporationUpdated: Feb 9, 2026Locations: 1
Eligibility criteria
Subject has an intracranial aneurysm (ruptured or unruptured) that can be treate... [+3]
Subject is currently enrolled in or plans to be enrolled in a concurrent drug or... [+3]