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Search / Trial NCT06924996

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

Launched by FENG GAO · Apr 10, 2025

Trial Information

Current as of July 27, 2025

Enrolling by invitation

Keywords

ClinConnect Summary

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 (ST...

Gender

ALL

Eligibility criteria

  • 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).

About Feng Gao

Feng Gao is a dedicated clinical trial sponsor committed to advancing medical research and improving patient outcomes through innovative therapeutic solutions. With a focus on rigorous scientific methodologies and ethical standards, Feng Gao collaborates with healthcare professionals and research institutions to facilitate the development and testing of novel treatments across various medical fields. By prioritizing patient safety and data integrity, the organization aims to contribute significantly to the advancement of healthcare and the discovery of effective interventions for unmet medical needs.

Locations

Beijing, , China

Patients applied

0 patients applied

Trial Officials

gao feng, professor

Study Chair

Beijing Tiantan Hospital

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported