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Post Market Registry Study of Intracranial Aneurysms Treated With Sugita Clipping Devices | Clinical Trials | Clareo Health

RECRUITING

Post Market Registry Study of Intracranial Aneurysms Treated With Sugita Clipping Devices

NCT06798740•Mizuho Corporation

View on ClinicalTrials.gov

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.

Eligibility

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

Inclusion Criteria

•Subject has an intracranial aneurysm (ruptured or unruptured) that can be treated with one of the proposed devices.
•Subject is adult, ≥18 years.
•As per national regulations, subject or subject's legally authorized representative (LAR) has signed written informed consent.
•Subject is willing to comply with scheduled visits and examinations per institutional standard of care.

Exclusion Criteria

•Subject is currently enrolled in or plans to be enrolled in a concurrent drug or device randomized study.
•Subject has a condition which will not allow him/her to comply with his/her post-procedure follow up per the institutional standard of care (medical condition, subject living abroad and unable to return for follow- up, e.g.).
•Subject does not meet IFU criteria of the subject device.
•Subject is a child, \<18 years.

Locations (1)

Universitätsklinikum Essen

Essen, Germany

Key Dates

Start Date

April 14, 2025

Primary Completion Date

February 14, 2027

Completion Date

February 14, 2033

Last Updated

February 9, 2026

Enrollment

150

ESTIMATED participants

Conditions

Brain Aneurysm

Interventions

Sugita Titanium Aneurysm Clip II

DEVICE

Contacts

Mai Hamayoshi

CONTACT

+81-3-3815-3180 m.hamayoshi@mizuho.co.jp

Aneurysm Study of Pipeline in an Observational Registry

NCT01557036

Brain Aneurysm

View study

Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: February 9, 2026Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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