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NCT Number: NCT06498323

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

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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 criteria

  • Diagnosed as Acute ischemic stroke with more than 4.5 hours of symptom onset or uncontained onset
  • Have contraindication for thrombolytic drugs

Treatment and study plan

Tenecteplase

Drug

Intravenous thrombolytic agents administration

Primary outcomes

  1. mRS Score

    Time frame: at 3 months

    mRS Score

Secondary outcomes

  1. NIHSS Score at 24 hrs

    Time frame: at 24 hours

    NIHSS Score at 24 hrs after intravenous tenecteplase

Study contacts

Contact information is provided by the study sponsor or research team.

Yongchai Nilanont

CONTACT

[email protected]

924245898

Sponsors and collaborators

Lead sponsor

Mahidol University

Other

Registry information

Official study title

Intravenous Tenecteplase Versus Alteplase for Acute Ischemic Stroke Treatment on Mobile Stroke Units, a Prospective Multicenter Randomized Controlled Trial

Important dates

Study start
2022
Primary completion
2025
Study completion
2025
First posted
Jul 12, 2024
Registry last updated
Jul 12, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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