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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-100
SponsorThe First Affiliated Hospital of University of Science and Technology of China

About this trial

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 criteria

Qualifiers

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.

Disqualifiers

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.

Trial design

Treatments tested in this trial

  • TNK plus standard medical treatment
  • standard medical management

Treatment groups

406 Participants
are divided into 2 treatment groups