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NCT07390032Not yet recruiting

The Efficacy and Safety of Endovascular Treatment for Acute Mild Basilar Artery Occlusion

The Efficacy and Safety of Endovascular Treatment for Acute Mild Basilar Artery Occlusion: A Multicenter, Prospective, Open-Label, Endpoint-Blinded, Randomized Controlled Clinical Trial

Source: ClinicalTrials.gov · Last updated 5 Feb 2026

Brief summary (registry, in English)

This study assesses the efficacy and safety of endovascular treatment for acute mild basilar artery occlusion within a multicenter, prospective, open-label, endpoint-blinded, randomized controlled clinical trial.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
230 (estimated)
First submitted
28 Jan 2026
Start date
1 Mar 2026
Primary completion date
31 Dec 2028
Lead sponsor
Feng Gao
Diseases
Stroke
NCT number
NCT07390032

What you commit to

  • Study type: Interventional
  • Planned participants: 230
  • From 1 Mar 2026 to the primary completion date, 31 Dec 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Any sign of intracranial hemorrhage (except microbleeds) on brain imaging prior to randomization
  • Enrolled in another drug or device trial or expected to participate in another drug or device treatment trial within the following 3 months
  • Acute cerebral infarction occurred within 48 hours after cardio cerebral vascular intervention or major surgery (patients over 48 hours can be included in the group)

Other illness

  • History of contraindication for contrast medium (except mild rash)
  • Refractory hypertension (defined as systolic blood pressure\>185 mmHg or diastolic blood pressure\>110 mmHg) that cannot be controlled by drug treatment
  • Patients whose life expectancy is less than 1 year (such as patients with malignant tumor, advanced cardiopulmonary disease, etc.)
  • Known to have dementia or psychiatric disease unable to complete neurological assessment and follow-up
  • It is known that patients with dementia or mental illness cannot complete neurological function assessment and follow-up
  • Any other condition (in the opinion of the site investigator) that inappropriate to participate this study

Lab values

  • Known hereditary or acquired bleeding tendency, lack of coagulation factors, or oral anticoagulants with INR\>1.5
  • Blood glucose\<2.8 or\>22.2 mmol/L; Platelet count\<100\*109/L, serum creatinine\>2.0 g/L (177 μ mol/L), or glomerular filtration rate\<30 ml/(min\*1.73 m2)

Other

  • Complete cerebellar infarct with significant mass effect, or bilateral thalamic infarction as evidenced by baseline neuroimaging
  • Known or highly suspected chronic occlusion of basilar artery
  • CTA/MRA/DSA confirmed occlusion of anterior and posterior circulation
  • Severe stenosis, arterial dissection, or excessive tortuosity of the extracranial or intracranial segments of the vertebral artery may result in the inability of interventional instruments to be successfully delivered or positioned
  • Current pregnant or breast-feeding
  • Central nervous system vasculitis has been diagnosed or clinically suspected

Who the study is looking for

  • Age≥18
  • Acute ischemic stroke in posterior circulation, the time from stroke onset (or finally found normal) to randomization was within 24 hours
  • Acute basilar artery occlusion confirmed by CTA,MRA,or DSA
  • NIHSS score≥2 points and\<10 points from the onset of the disease to before randomization
  • Posterior circulation large core infarction:NCCT or DWI showed pc-ASPECTS≥6, or Pons-Midbrain Index (PMI)\<3
  • No significant functional disability before stroke (mRS≤2 points)
  • Each patient or their legal representative must provide written informed consent before enrolment

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Beijing Tiantan Hospital,Capital Medical University
Coordinator of this site? Confirm its status
BeijingChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.