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

NCT06798740 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2026-02-09

No results posted yet for this study

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

  • Brain Aneurysm

Interventions

DEVICE

Sugita Titanium Aneurysm Clip II

Aneurysm clipping is a surgical procedure used to treat brain aneurysms.

Sponsors & Collaborators

  • Mizuho Corporation

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-04-14
Primary Completion
2027-02-14
Completion
2033-02-14

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06798740 on ClinicalTrials.gov