Clin2
NCT05880680Possibly a fitRecruiting

SEAL device registry for certain brain aneurysms treated through blood vessels

AneurysmAneurysm, Ruptured

Part of Heart & circulation clinical trials.

This study follows people who have a brain aneurysm that can be treated using the SEAL device placed from inside a blood vessel. It aims to track how well the treatment works and how safely it can be used in real-world care.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
200 people
Ages
18 years to 80 years
Study type
Observational

Who can take part

  • You are between 18 and 80 years old when screened.
  • You have an aneurysm (either unruptured needing treatment or a ruptured aneurysm) that doctors judge is suitable for the SEAL device.
  • The aneurysm must be a sac-like (saccular) type, located at a branching spot or sidewall, and be 2.5 to 20 mm wide.
  • For ruptured aneurysms: you must be neurologically stable, not needing an external brain drain (EVD) before enrollment, and have limited disability before the event.
  • The treatment plan must not require other implanted devices ahead of time (except if needed for safety).
  • You must be able to follow all study visits and have consent paperwork signed by you or a legal representative.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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