Trials / Recruiting
RecruitingNCT06798740
Post Market Registry Study of Intracranial Aneurysms Treated With Sugita Clipping Devices
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 150 (estimated)
- Sponsor
- Mizuho Corporation · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Sugita Titanium Aneurysm Clip II | Aneurysm clipping is a surgical procedure used to treat brain aneurysms. |
Timeline
- Start date
- 2025-04-14
- Primary completion
- 2027-02-14
- Completion
- 2033-02-14
- First posted
- 2025-01-29
- Last updated
- 2026-02-09
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT06798740. Inclusion in this directory is not an endorsement.