Intravenous TNK vs TPA for AIS Treatment on MSU,a Prospective Multicenter RCT

Last updated: July 5, 2024
Sponsor: Mahidol University
Overall Status: Active - Recruiting

Phase

4

Condition

Stroke

Blood Clots

Cardiac Ischemia

Treatment

tenecteplase

Clinical Study ID

NCT06498323
376/2565(IRB1)
  • Ages > 18
  • All Genders

Study Summary

Acute ischemic stroke is one of the devastating diseases that increase hospitalization, disabilities, and deaths worldwide. Current treatment with intravenous thrombolytic agent can help reduce disabilities and improve quality of life. Intravenous Alteplase is proven benefit and now used as the first-line drug for acute ischemic stroke with symptom onset less than 4.5 hours and without contraindications.

Tenecteplase, a genetically engineered tissue-type plasminogen activator, has been questioned to treat acute ischemic stroke instead of intravenous alteplase. Tenecteplase has more advantages over alteplase including higher fibrin specificity, longer half-life and easier to administer as a single intravenous bolus. The efficacy and safety of intravenous tenecteplase has been studied recently. In 2017, A phase 3 randomized open-label, blinded trial (NOR-TEST) 6 showed that there were no significant differences in efficacy and safety between tenecteplase and alteplase in mild stroke patients. A study in 2020, in the setting of acute large artery occlusion, Tenecteplase resulted in a better 90-day neurological outcome and provided more benefits in reperfusion before endovascular thrombectomy10. Regarding safety concerns, tenecteplase showed no significant higher incidence of intracerebral hemorrhage. Administration, tenecteplase might be better in the setting of the case on mobile stroke units. Assuming, earlier reperfusion by thrombolytic drug may have improved patient's neurologic outcomes. We aim to compare the efficacy and safety between intravenous tenecteplase and alteplase in acute ischemic stroke patients given on mobile stroke units within 4.5 hours after symptom onset.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Diagnosed as Acute ischemic stroke within 4.5 hr of symptom onset

  • Age > 18 years old

  • No contraindication for thrombolytic drug

  • Informed consent from patients

Exclusion

Exclusion Criteria:

  • Diagnosed as Acute ischemic stroke with more than 4.5 hours of symptom onset oruncontained onset

  • Have contraindication for thrombolytic drugs

Study Design

Total Participants: 160
Treatment Group(s): 1
Primary Treatment: tenecteplase
Phase: 4
Study Start date:
August 03, 2022
Estimated Completion Date:
August 31, 2025

Connect with a study center

  • Siriraj Stroke Center,Siriraj Hospital

    Bangkok, 10700
    Thailand

    Active - Recruiting

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.