Tenecteplase for Acute Ischemic Stroke Within 4.5 to 6 Hours of Onset (EXIT-BT2)
Condition(s) studied
Investigational drug(s) / intervention(s)
Tenecteplase: intravenous tenecteplase (0.25 mg/kg, a single bolus over 5 to 10 seconds, a maximum of 25 mg).
Study summary
To date, the benefit of intravenous thrombolysis is confined within 4.5 hours of onset for acute ischemic stroke (AIS) patients without advanced neuroimaging selection. Unpublished pilot EXIT-BT (EXtending the tIme window of Thrombolysis by ButylphThalide up to 6 Hours after onset) suggest the safety, feasibility and potential benefit of intravenous tenecteplase (TNK) in AIS within 4.5 to 6 hours of onset. The current study aims to investigate the efficacy and safety of TNK for AIS within 4.5 to 6 hours of onset.
Eligibility
Primary outcome measure(s)
- proportion of modified Rankin Scale (mRS) 0-1 — 90±7 days
The minimum and maximum values of mRS are 0 and 6, respectively; higher score mean a worse outcome
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Hui-Sheng Chen | Shenyang | None Selected | Recruiting |
| Department of Neurology, General Hospital of Northern Theater Command | Shenyang | China | Recruiting |
More General Hospital of Shenyang Military Region trials in China
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06010628 on ClinicalTrials.gov ↗ ← All trials in China