Rescue Intracranial Stenting in Acute Ischemic Stroke (RISIS)

Can Tho Stroke International Services Hospital

Status: Completed

Conditions: Intracranial Atherosclerosis; Ischemic Stroke; Stent Occlusion; Cerebral Ischemia; Stent Stenosis; Thrombotic Stroke, Acute; Intracranial Hemorrhages; Acute Stroke; Stroke, Ischemic

Treatments: Procedure: Rescue intracranial stenting

Study type: Interventional

Funder types: Other

Identifiers

NCT04986774

Can Tho SIS Hospital

Details and patient eligibility

About

In acute ischemic stroke caused by intracranial large vessel occlusion, rescue intracranial stenting has been recently a treatment option to achieve recanalization in patients with the failure of mechanical thrombectomy. Nevertheless, there are few studies supporting this beneficial treatment in two cerebral circulations. We aimed to analyse whether the use of rescue intracranial stenting would improve prognosis of patients at 3 months.

Full description

In Asia population, large intracranial arterial stenosis lesion accounts for more than 30% in common causes of ischemic stroke, compares with about 10% in Caucasian population every year. Normally, in human brain, there are about 130 billion neurons but they are lost equivalent to their losses in approximately 3.6 years of normal aging in case of a large vessel ischemic stroke untreated each hour. Consequently, after the success of 5 randomized controlled trials about the mechanical thrombectomy, which have been done from December 2010 to December 2014, all of guidelines recommended this technique as the first-line treatment in acute ischemic stroke. However, the HERMES meta-analysis showed that revascularisation failure ratio 28.9% in patients older than 80 years. Recently, in case of mechanical thrombectomy failure, many studies suggested the rescue intracranial stenting could be alternative urgently needed treatment to achieve permanent recanalization which is one of the most important factors impacting on clinical outcomes after acute ischemic stroke. Hence, the aims of our study were to assess both the "non-poor" outcome at 3 months and the symptomatic intracerebral hemorrhage relating to procedure in patients receiving rescue intracranial stenting.

Enrollment: 85 patients

Sex: All

Ages: 20 to 105 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Evidence of intracranial large vessel occlusion.
• Absence of intracranial hemorrhage.
• Severe stenosis or reocclusion after mechanical thrombectomy.

Exclusion criteria

• Tandem lesion.
• Loss to follow-up after discharge.
• A severe or fatal combined illness before acute ischemic stroke.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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85 participants in 1 patient group

Rescue Intracranial Stenting (RIS)

Experimental group

Description:

RIS in Acute Ischemic Stroke caused by intracranial large vessel occlusion

Treatment:

Procedure: Rescue intracranial stenting