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Efficacy and Safety of Endovascular Thrombectomy in Acute Ischemic Stroke With Posterior Circulation Large Infarct

F

Feng Gao

Status

Invitation-only

Conditions

Posterior Circulation Large Infarct
Acute Basilar Artery Occlusion

Treatments

Procedure: Endovascular Thrombectomy (EVT)

Study type

Observational

Funder types

Other

Identifiers

NCT06924996
KY2023-106-02

Details and patient eligibility

About

The purpose of this study is to evaluate whether endovascular thrombectomy (EVT) combined with best medical management (BMM) leads to better functional outcomes than BMM alone in patients with acute basilar artery occlusion with posterior circulation large infarct.

Full description

This study is a multicenter, prospective, cohort study that prospectively enrolled consecutive patients with acute basilar artery occlusion and large core infarction in the posterior circulation, confirmed by imaging (CTA/MRA/DSA). Written informed consent was obtained from all participants or their legal representatives prior to enrollment. Patients were divided into the best medical management (BMM) group and the endovascular thrombectomy (EVT) group according to the treatment they received. This study adhered to the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) guidelines.

Enrollment

500 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age 18-80 years old;
  2. Acute ischemic stroke in the posterior circulation, the onset of stroke (or last well known) to the enrollment time within 24 hours;
  3. CTA/MRA/DSA confirmed acute basilar artery occlusion;
  4. Posterior circulation large infarct: NCCT or DWI showed pc-ASPECTS ≤ 5 points, or pontine midbrain index (PMI) ≥ 3 points;
  5. NIHSS score ≥10 points after the onset of the stroke and before enrollment;
  6. Able to live independently before the onset of the disease (mRS score ≤2 points);
  7. The subject or legal representative is able to sign the informed consent form.

Exclusion criteria

  1. Intracranial hemorrhage (except microhemorrhage) on CT/MRI ;
  2. CT/MRI revealed large infarction in the cerebellar hemisphere, with significant mass effect causing compression of the fourth ventricle or brainstem;
  3. CT or MRI showed bilateral complete thalamic infarction;
  4. Occlusion of anterior and posterior circulation arteries confirmed by CTA/MRA/DSA;
  5. The presence of intracranial tumors (except for small meningiomas and cerebral aneurysms with a diameter of <3mm);
  6. Patients with known or highly suspected chronic basilar artery occlusion.;
  7. Known severe allergy to contrast agents (except for mild rash);
  8. Refractory hypertension (defined as systolic blood pressure > 185 mmHg or diastolic blood pressure >110 mmHg) that cannot be controlled by drug therapy;
  9. Known pregnant or lactating females, or positive pregnancy test before enrollment;
  10. Acute cerebral infarction within 48 hours after cardiovascular and cerebrovascular intervention or major surgery (patients more than 48 hours can be enrolled).

Trial design

500 participants in 2 patient groups

Endovascular Thrombectomy (EVT)
Description:
The EVT group would include the following interventions: stent-retriever thrombectomy, aspiration thrombectomy, balloon angioplasty and/or stenting, intra-arterial medication administration, or a combination of these approaches.
Treatment:
Procedure: Endovascular Thrombectomy (EVT)
Best Medical Management (BMM)
Description:
BMM was tailored according to institutional guidelines and included intravenous thrombolysis (IVT), antiplatelet therapy, anticoagulation, or multimodal combinations.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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