Mechanical thrombectomy using large aspiration catheter for acute ischemic stroke

Mechanical thrombectomy using large aspiration catheter for acute ischemic stroke - REACT AIS Registry

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000042232

Enrollment

1380

Registered

2020-10-30

Start date

2020-10-30

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

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1 acute ischemic stroke patient treated mechanical thrombectomy using REACT and/or Solitaire FR within 24hrs after stroke. 2 occluded ICA, M1, M2-3, VA-BA

Exclusion criteria

Exclusion criteria: 1 patient used non-approval devices 2 patient occluded 2 or more major vessels, ICA, VA-BA 3 patient don't want provide their medical informations to the study group

Design outcomes

Primary

Measure	Time frame
rate of recanalization more than mTICI2c	—

Secondary

Measure	Time frame
Efficacy 1 the best recanalization rate; more than mTICI2c 2 recanalization rate more than mTICI2c of the first thrombectomy 3 the best recanalization rate of the first thrombectomy 4 mRS 0-2 at 90days after intervention Safety 1 rate of intracranial hemorrhage within 24hr after intervention 2 rate of symptomatic intracranial hemorrhage within 24hr after intervention 3 symptomatic vasospasm during intervention 4 device malfunction and advance event related device	—

Measure

Time frame

Efficacy 1 the best recanalization rate; more than mTICI2c 2 recanalization rate more than mTICI2c of the first thrombectomy 3 the best recanalization rate of the first thrombectomy 4 mRS 0-2 at 90days after intervention Safety 1 rate of intracranial hemorrhage within 24hr after intervention 2 rate of symptomatic intracranial hemorrhage within 24hr after intervention 3 symptomatic vasospasm during intervention 4 device malfunction and advance event related device

—

Countries

Japan

Contacts

Public ContactChiaki Sakai

Kobe City Medical Center General Hospital Center for Clinical Research and Innovation

chiakmk@cronos.ocn.ne.jp078-302-4321

Outcome results