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Randomized study of endovascular therapy with versus without intravenous tissue plasminogen activator in acute stroke with ICA and M1 occlusion - A prospective, multicenter, randomized trial

Randomized study of endovascular therapy with versus without intravenous tissue plasminogen activator in acute stroke with ICA and M1 occlusion - A prospective, multicenter, randomized trial - Efficiency of alone endovascular therapy for acute ischemic stroke patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000021488
Enrollment
200
Registered
2016-04-01
Start date
2017-01-01
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

Interventions

Endovascular therapy Endovascular therapy intravenous tissue plasminogen

Sponsors

Nippon Medical School
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients of from 18 to 85 years old 2.Continued clinical symptoms in patoents with acute cerebral infarction 3.Pre mRS within 2 4.Patients with ICA or M1 occlusion and be able to puncture within 4 hours. 5.DWI-ASPECTS more than 5 or ASPECTS more than 6 at pre endovascular therapy 6.NIHSS more than 6 7.Research consent have been obtained in writing from the person or alternative person

Exclusion criteria

Exclusion criteria: 1.Patients with a hypersensitivity to contrast 2.Past history of puncture artery hemostasis 3.Patients with severe urine function 4.A lactating or pregnant patients 5.Patient expected life expectancy within 90 days 6.Ineligible for tPA therapy patients 7.Patient deemed unfit to conduct this testing responsible physician or trial division

Design outcomes

Primary

MeasureTime frame
Rate of Modified Rankin Scale 0-2 at 90 days after onset. (Noninferior)

Secondary

MeasureTime frame
Rate of asymptomatic and symptomatic intracranial hemorrhage at 24 hours after onset.

Countries

Japan

Contacts

Public ContactKENTARO SUZUKI

Nippon Medical School Neurological Science

kentarow@nms.ac.jp03-3822-2131

Outcome results

None listed

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