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NCT07699029Recruiting

Endovascular Treatment for Posterior Circulation Ischemic Stroke Post 1 Day (24 Hours)

Endovascular Treatment for Posterior Circulation Ischemic Stroke Post 1 Day (24 Hours) A Randomized Controlled Clinical Trial On Efficacy

Source: ClinicalTrials.gov · Last updated 30 Jul 2026

Brief summary (registry, in English)

To evaluate the efficacy and safety of endovascular therapy for posterior circulation ischemic stroke presenting more than 24 hours after symptom onset.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
244 (estimated)
First submitted
7 Jul 2026
Start date
16 Jul 2026
Primary completion date
1 Aug 2029
Lead sponsor
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Diseases
Stroke
NCT number
NCT07699029

What you commit to

  • Study type: Interventional
  • Planned participants: 244
  • From 16 Jul 2026 to the primary completion date, 1 Aug 2029
  • 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, not your situation.

Who cannot take part

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

Prior treatment

  • Evidence of vascular recanalization prior to randomization
  • Attempted use of a neurothrombectomy device to remove the clot prior to randomization
  • Currently participating in a study involving other investigational drugs or devices

Other illness

  • Hemorrhage on CT or MRI
  • Based on the judgment of the treating physician, the patient is considered unlikely to benefit from the trial (e.g., advanced dementia, severe pre-stroke disability (mRS ≥ 2), or high risk of early mortality)
  • Major comorbidities that may interfere with outcome assessment and follow-up (e.g., severe heart failure, renal failure, etc.).
  • Uncontrolled seizures at the time of stroke onset, if they interfere with obtaining an accurate baseline NIHSS
  • Posterior circulation Acute Stroke Prognosis Early CT score (pc-ASPECTS) \< 6 on non-contrast CT or CT angiography source images or MR with diffusion-weighted imaging
  • Severe, persistent hypertension (systolic blood pressure \> 220 mmHg or diastolic blood pressure \> 120 mmHg)
  • Known allergies to iodine, heparin, anesthetics, or other explicit contraindications to the endovascular treatment procedure
  • Other serious, progressive, or end-stage diseases (as determined by the investigator) or a life expectancy of less than 6 months
  • Any other conditions that the investigator believes may interfere with the endovascular procedure or pose significant risk to the subject during the procedure

Lab values

  • Baseline platelet count \<50,000/uL
  • Known hereditary or acquired bleeding disorders, coagulation factor deficiencies, or recent oral anticoagulant therapy with an International Normalized Ratio (INR) \> 3

Other

  • Complete cerebellar infarct with significant mass effect and compression of the fourth ventricle,or bilateral thalamic infarction on CT or MRI
  • Suspected purulent embolism, with a suspicion of bacterial endocarditis
  • Pregnancy
  • Evidence of intracranial tumor on CT or MRI (excluding meningioma)
  • CTA/MRA showing excessive tortuosity of the cervical vessels, which may interfere with endovascular treatment
  • Suspicion of aortic dissection based on medical history and CTA/MRA findings

Who the study is looking for

  • Age ≥ 18 years old
  • Baseline NIHSS score of 4 or higher, maintained prior to randomization
  • Stroke onset or more than 24 hours since the last known good state, but within 14 days
  • CTA/MRA/DSA confirmed occlusion of the responsible vessel in basilar artery or intracranial segments of both vertebral arteries (V4)
  • Modified Rankin Scale (mRS) score of 0 or 1 pre-stroke
  • The subject or their legally authorized representative has signed the informed consent form for the study

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. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Union Hospital Affiliated to Tongji Medical College, Huazhong University of Science and Technology
Coordinator of this site? Confirm its status
WuhanChinaRecruiting

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