Stroke Clinical Trials

Find Stroke Clinical Trials Near You

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

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
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
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 100
Healthy Volunteers: f
View:

• 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.

Locations
Other Locations
China
The First Affiliated Hospital of the University of Science and Technology of China
RECRUITING
Hefei
Contact Information
Primary
Wei Hu MD,PhD
andinghu@ustc.edu.cn
+86055162284313
Time Frame
Start Date: 2025-11-05
Estimated Completion Date: 2027-12-30
Participants
Target number of participants: 406
Treatments
Active_comparator: standard medical management
standard medical management
Experimental: TNK 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.
Related Therapeutic Areas
Sponsors
Leads: The First Affiliated Hospital of University of Science and Technology of China

This content was sourced from clinicaltrials.gov

Similar Clinical Trials