NCT06510634
Enrolling By Invitation
Not Applicable
Effectiveness and Safety of Endovascular Treatment vs. Best Medical Treatment in Patients With Vertebrobasilar Artery Occlusion Presenting Beyond 24 Hours of Last Known Well:a Prospective, Multicenter Registry Study
Tianjin Huanhu Hospital1 site in 1 country236 target enrollmentJune 1, 2019
ConditionsStroke, Ischemic
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Stroke, Ischemic
- Sponsor
- Tianjin Huanhu Hospital
- Enrollment
- 236
- Locations
- 1
- Primary Endpoint
- proportion of patients with Modified ranking scale (mRS) (0-3) at 90 days
- Status
- Enrolling By Invitation
- Last Updated
- last year
Overview
Brief Summary
Endovascular thrombectomy (EVT) for posterior circulation occlusion is generally performed within a window of less than 24 hours from the time the patient was last known well (LKW). The efficacy and safety of EVT beyond the 24-hour window remain uncertain.
Investigators
Ming Wei
Chief Physician
Tianjin Huanhu Hospital
Eligibility Criteria
Inclusion Criteria
- •age≥18 years.;
- •blockage in the vertebrobasilar artery, including the vertebral artery or basilar artery, determined using computed tomographic angiography (CTA)/ magnetic resonance angiography (MRA)/digital subtraction angiography (DSA);
- •VBAO occurrence more than 24 hours from LKW;
- •none to mild premorbid disability defined by modified Rankin Scale (mRS) score ≤2;
- •informed consent before enrollment in the clinical trials.
Exclusion Criteria
- •neuroimaging evidence of cerebral hemorrhage on presentation;
- •lack of follow up information on outcomes at 90 days
- •serious, advanced, or terminal illness.
Outcomes
Primary Outcomes
proportion of patients with Modified ranking scale (mRS) (0-3) at 90 days
Time Frame: 90(±14)days
A 0-6 scale running from perfect health without symptoms to death.
Secondary Outcomes
- Mortality within 90 days(90(±14)days)
- distribution of patients with Modified ranking scale (mRS) (0-3) at 90 days(90(±14)days)
- Incidence of symptomatic intracranial haemorrhage(90(±14)days)
Study Sites (1)
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