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Hybrid mechanical thrombectomy for acute ischemic stroke using intermediate aspiration catheter and Trevo stent

Hybrid mechanical thrombectomy for acute ischemic stroke; Comparison with traditional mechanical thrombectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0004116
Enrollment
100
Registered
2019-07-03
Start date
2019-06-20
Completion date
Unknown
Last updated
2019-07-17

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

Conditions

None listed

Interventions

Procedure/Surgery : At our hospital, we designed a hybrid mechanical thrombectomy using catheter aspiration and stent retriever simultaneously as follows: 1) a stent (Trevo, Stryker Neurovascular, Fre
2) subsequently, the intermediate catheter (large bore aspiration catheter) is navigated to the proximal portion of thrombus burden according to the deployed stent system
3) proximal flow is arrested by balloon guide catheter
and 4) the intermediate catheter and stent are removed simultaneously under continuous negative pressure with a large syringe.

Sponsors

Inje University Haeundae Paik Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) acute ischemic stroke with symptoms 2) large artery occlusions confirmed by either CT or MR angiography 3) period of less than 24 hours from the LNT to treatment 4) treated by MT using a hybrid MT or traditional MT.

Exclusion criteria

Exclusion criteria: 1) posterior circulation occlusion 2) anterior cerebral artery occlusion 3) proximal internal carotid artery (ICA) 4) patients whose MT was switched from hybrid MT to traditional MT or from traditional MT to hybrid MT

Design outcomes

Primary

MeasureTime frame
Clinical outcome;Radiological outcome

Secondary

MeasureTime frame
Procedure time;Attempt number

Countries

Korea, Republic of

Contacts

Public ContactSung-Chul Jin

Inje University Haeundae Paik Hospital

kusmal@hanmail.net+82-51-797-0840

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026