Brain aneurysm clip safety under review in new registry study
NCT ID NCT06798740
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows 150 adults with brain aneurysms who are treated with Sugita aneurysm clips. The goal is to see how safe and effective the clips are in real-world use over 5 years. Researchers will track how well the aneurysm is closed and any side effects. This is an observational registry, not a test of a new treatment.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
About 150 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Apr 2025
- Expected to finish
-
Feb 2033
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Subjects who have an intracranial aneurysm (ruptured or unruptured) that the physician intends to treat with the subject device(s)
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Brain aneurysm are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Universitätsklinikum Essen
RECRUITINGEssen, D- 45122, Germany
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- AI plus ultrasound could catch heart and lung decline before it turns critical
- Real-World data on brain aneurysm device could improve patient safety
- Massive biobank aims to predict which brain aneurysms will rupture
- New device aims to seal brain aneurysms before they burst
- New brain aneurysm device gets first human test
- 5,000-Patient study to see which brain aneurysm devices work best