RecruitingNot ApplicableNCT07094763

Efficacy and Safety of Tenecteplase Intravenous Thrombolysis in Acute Posterior Circulation Ischemic Stroke Within 4.5-24 Hours After Onset

Efficacy and Safety of Tenecteplase Intravenous Thrombolysis in Acute Posterior Circulation Ischemic Stroke Within 4.5-24 Hours After Onset: A Multicenter, Prospective, Randomized, Open-Label, Blinded Endpoint Trial


Sponsor

The First Affiliated Hospital of University of Science and Technology of China

Enrollment

406 participants

Start Date

Nov 5, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This study aims to evaluate the efficacy and safety of tenecteplase (TNK) intravenous thrombolysis within the extended time window (4.5 to 24 hours) in patients with acute posterior circulation ischemic stroke.


Eligibility

Min Age: 18 YearsMax Age: 100 Years

Inclusion Criteria7

  • Age ≥18 years.
  • Meeting at least one of the following criteria: acute posterior circulation ischemic stroke confirmed by MRI; symptomatic stenosis or occlusion of a posterior circulation large vessel on vascular imaging (CTA/MRA/DSA); perfusion imaging demonstrating clinically relevant hypoperfusion in the posterior circulation territory.
  • Onset time between 4.5-24 hours (for wake-up stroke or unwitnessed stroke, onset time is defined as the midpoint between last known well and symptom detection).
  • NIHSS score>3.
  • PC-ASPECTS ≥7 (if discrepancy exists between DWI and CT findings, CT assessment takes precedence).
  • Pre-stroke mRS ≤1.
  • Signed informed consent by the patient or legally authorized representative.

Exclusion Criteria18

  • Contraindication to tenecteplase or its components.
  • Planing to receive endovascular therapy with thrombectomy, angioplasty or stenting whin 3 months.
  • Acute anterior circulation infarction confirmed by MRI, anterior circulation large vessel occlusion on vascular imaging (CTA/MRA/DSA), or anterior circulation hypoperfusion on perfusion imaging.
  • History of intracranial hemorrhage.
  • Stroke, myocardial infarction, severe traumatic brain injury, or intracranial/spinal surgery within the preceding 3 months.
  • Intracranial tumor, arteriovenous malformation (AVM), or giant aneurysm.
  • Active internal bleeding, major surgery, trauma, gastrointestinal/urinary tract bleeding within 3 weeks.
  • Non-compressible arterial puncture within 1 week.
  • Suspected aortic dissection.
  • Clinically significant bleeding or coagulopathy, including: Warfarin use with INR >1.7 or PT >15 s; Low-molecular-weight heparin within 24 hours; Direct oral anticoagulants within 48 hours; Laboratory abnormalities (e.g., APTT >40 s).
  • Platelet dysfunction or platelet count <100×10⁹/L.
  • Uncontrolled hypertension (systolic BP >180 mmHg or diastolic BP >110 mmHg unresponsive to antihypertensive therapy).
  • Uncontrolled hypoglycemia/hyperglycemia (<50 mg/dL \[2.8 mmol/L\] or >400 mg/dL \[22.2 mmol/L\]).
  • Pregnancy or lactation.
  • A life expectancy of less than three months.
  • Participation in other clinical trials within 3 months or ongoing trial enrollment.
  • Inability to follow up (e.g., no fixed residence, overseas patients).
  • Patient deemed unsuitable for the trial by site investigator.

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Interventions

DRUGTNK plus standard medical treatment

Patients in the TNK treatment group will receive TNK intravenous thrombolysis and the usual dosage for TNK intravenous thrombolysis is 0.25mg/Kg, with a maximum of 25mg.

DRUGstandard medical management

standard medical management


Locations(1)

The First Affiliated Hospital of the University of Science and Technology of China

Hefei, China

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NCT07094763


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