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Triage of Patients Presenting Beyond 24 Hours With Ischemic Stroke Due to Vertebrobasilar Artery Occlusion

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

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06510634
Acronym
VBAO-LATE
Enrollment
236
Registered
2024-07-19
Start date
2019-06-01
Completion date
2028-03-31
Last updated
2025-02-28

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

Conditions

Stroke, Ischemic

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.

Interventions

OTHEREndovascular Therapy

Endovascular therapy, as an adjunct to standard stroke therapy, may be beneficial for a very select population of patients who present with an acute ischemic stroke and have a proven large, proximal occlusion on imaging. Endovascular therapy includes any one or more of the following: Intra-arterial thrombolytic therapy, aspiration, stent retrieval, or a combination of multiple mechanical devices.

Sponsors

Tianjin Huanhu Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years

Inclusion criteria

1. age≥18 years.; 2. 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); 3. VBAO occurrence more than 24 hours from LKW; 4. none to mild premorbid disability defined by modified Rankin Scale (mRS) score ≤2; 5. informed consent before enrollment in the clinical trials.

Exclusion criteria

1. neuroimaging evidence of cerebral hemorrhage on presentation; 2. lack of follow up information on outcomes at 90 days 3. serious, advanced, or terminal illness.

Design outcomes

Primary

MeasureTime frameDescription
proportion of patients with Modified ranking scale (mRS) (0-3) at 90 days90(±14)daysA 0-6 scale running from perfect health without symptoms to death.

Secondary

MeasureTime frameDescription
distribution of patients with Modified ranking scale (mRS) (0-3) at 90 days90(±14)daysA 0-6 scale running from perfect health without symptoms to death.
Mortality within 90 days90(±14)daysmortality of any causes.
Incidence of symptomatic intracranial haemorrhage90(±14)daysSymptomatic intracranial hemorrhage was characterized as any type of intracranial hemorrhage observed on follow-up imaging between 22 and 36 hours and 7 days after stroke onset, accompanied by an increase of at least 4 points on the NIHSS from baseline or the lowest value within 7 days, or resulting in mortality.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026