Rescue Endovascular Therapy for Progressive Acute Mild Ischemic Stroke With Large Vascular Occlusion

• Status: Recruiting
• Trial end date: 2026-03-30
• Target enrollment: 0
• Participant gender: All

Summary

Endovascular therapy (EVT) added on best medical management is currently recommended in acute large vascular occlusion (LVO) stroke patients with National Institutes of Health Stroke Scale (NIHSS) score >5. Thus, a sizeable fraction of patients with a minor stroke that do not undergo cerebrovascular screening may experience an early neurological deterioration (END) due to LVO, possibly leading to poor long-term functional outcome. However, whether these patients may still benefit from a rescue EVT is unknown, especially in a late window (>24 hours). In this study, the investigators assume that best medical management plus EVT might be superior than best medical management alone in a late window for minor stroke patients who have experienced an LVO and END. The primary objective of the study was to establish the safety and efficacy of EVT in a late window for minor stroke patients in the anterior circulation who experienced an LVO and END.

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: First Affiliated Hospital of Wannan Medical College
• Collaborator: The First Affiliated Hospital of Anhui Medical University

Criteria

Inclusion Criteria:

General Inclusion Criteria：

• Age ≥ 18 years；

• Presenting with symptoms consistent with an AIS and the initial NIHSS score <6 points；

• Symptom progression within 7 days of first onset；

• Randomization can be finished > 24 hours of stroke onset (stroke onset time is defined as last known well time)；

• Symptom progression to randomization time ≤ 24 hours；

• NIHSS score before randomization ≥ 6 points；

• Informed consent signed.

Specific Neuroimaging Inclusion Criteria

• CTA or MRA proved occlusion of Internal Carotid Artery (ICA) terminal or M1 segment of Middle Cerebral Artery;

• The progression of symptoms is caused by the recurrence of cerebrovascular diseases in the same vascular region, or the pathogenesis is caused by reduced blood flow perfusion;

• NCCT ASPECTS before randomization ≥ 6 CTP or MRP assessment shows low perfusion in the target vessel area (Tmax>6S ≥ 70ml), and meets the following criteria: core infarction volume is less than 50ml, mismatch rate is greater than or equal to 1.2, and mismatch volume is greater than 10ml.

Exclusion Criteria:

• Pre-stroke mRS score >1;

• Imaging confirms the progression of symptoms caused by intracranial hemorrhage, brain edema, or other clear causes;

• The target vessel may have factors that may prevent it from completing endovascular treatment, such as a diameter less than 1.5mm, a tortuous vascular pathway, difficulty in reaching the target position with instruments, or difficulty in recovery;

• Severe stenosis or occlusion of multiple blood vessels;

• Combined with untreated intracranial aneurysms, intracranial tumors (excluding small meningiomas), or intracranial vascular malformations;

• Intracranial hemorrhage within 6 months, including cerebral parenchymal hemorrhage, ventricular hemorrhage, and subarachnoid hemorrhage;

• Have had gastrointestinal or urinary system bleeding, acute myocardial infarction, traumatic brain injury, or undergone major surgical procedures within the past month;

• Known hemorrhagic tendency (including but not limited to): Baseline platelet count <40×109/L; on anticoagulant therapy with warfarin and International Normalized Ratio (INR) > 2 (Patients with no history or suspected coagulopathy do not need to wait for laboratory results of INR or APTT prior to enrollment) Severe heart, liver, kidney function damage or other severe late stage diseases of the system;

• Known allergies to treatment related drugs such as iodine contrast agents, etc; Known severe allergy (more than a rash) to contrast media uncontrolled by medications;

• Refractory hypertension (defined as persistent systolic blood pressure >185 mmHg or diastolic blood pressure >110 mmHg);

• Uncontrolled blood sugar abnormalities (less than 2.8mmol/l or greater than 22.2mmol/l);

• Females who are pregnant, or those of child-bearing potential with positive urine or serum beta Human Chorionic Gonadotropin (HCG) test;

• The expected survival time is less than 1 year (such as complicated with malignant tumor, serious heart and lung diseases, etc.)

• Participation in other interventional randomized clinical trials that may confound outcome assessment of the trial

• Other circumstances that the investigator considers inappropriate for participation in the trial or that may pose significant risks to patients (such as inability to understand and/or follow the study procedures and/or follow up due to mental disorders, cognitive or emotional disorders)