Safety and efficacy of the stabilizer device

Safety and efficacy of the stabilizer device using in endovascular therapy for cerebral aneurysm

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-jRCTs052210098

Enrollment

Registered

2021-10-04

Start date

2021-10-25

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cerebral aneurysm

Interventions

Assisting delivery with stabilizer devices for patients who have difficulty delivering catheters to the treatment site during endovascular treatment,

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1)Patients who are scheduled to have a flow divertor or coil-assisted stent for cerebral aneurysm 2) Patients who are expected to have difficulty delivering the catheter to the treatment site. 3)Patients aged between 20years and 80years old at the time of concent acquisition 4)Patients who consented to the study in writing

Exclusion criteria

Exclusion criteria: 1)A history of hypersensitivity to nickel or titanium 2)A patient who is judged by the principal investigator to be inappropriate in this study

Design outcomes

Primary

Measure	Time frame
hemorrhagic stroke	—

Secondary

Measure	Time frame
ischemic stroke,success of exchange catheters,arterial dissection,vasospasm,adverse event ,Delivery of catheter to treatment site	—

Contacts

Public ContactUtako Shirono

Kobe City Medical Center General Hospital

ushirono@kcho.jp+81-78-302-4321

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026