Effectiveness of SOFIA PLUS for acute ischemic stroke caused by cerebral large artery occlusion

Effectiveness of SOFIA PLUS for acute ischemic stroke caused by cerebral large artery occlusion - Effectiveness of SOFIA PLUS

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000022791

Enrollment

Registered

2016-07-30

Start date

2016-08-01

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

Acute ischemic stroke caused by cerebral large artery occlusion

Interventions

Sofia PLUS

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients with acute ischemic stroke caused by cerebral large artery occlusion within 8 hours after the onset of the symptom

Exclusion criteria

Exclusion criteria: Patients with large ischemic stroke diagnosed by CT or MRI.

Design outcomes

Primary

Measure	Time frame
Improvement of National institutes of health stroke scale at 90 days after the treatment	—

Secondary

Measure	Time frame
Time from puncture to recanalization Degree of scattering of thrombus on desital subtraction angiography The amount of retrieved thrombus Improvement of ischemic stroke area	—

Countries

Japan

Contacts

Public ContactShinichi Yoshimura

Hyogo College of Medicine Department of Neurosurgery

shinyoshi@gmail.com0798-45-6455

Outcome results

None listed

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