A Medical Device to Treat Wide-Neck Brain Aneurysms

NCT05550571 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2025-04-30

No results posted yet for this study

Summary

The study aims to evaluate the safety and probable benefit of a medical device to treat wide-neck ruptured brain aneurysms.

Conditions

  • Ruptured Cerebral Aneurysm

Interventions

DEVICE

Nautilus Intrasaccular Bridging System

Patients will be treated with the Nautilus, then followed-up for 12 months

Sponsors & Collaborators

  • EndoStream Medical

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-12-17
Primary Completion
2026-07-01
Completion
2026-10-01
FDA Device
Yes

Countries

  • United States
  • Bulgaria

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 NCT05550571 on ClinicalTrials.gov