Intravenous Tenecteplase for Acute Ischemic Stroke Within 4.5 to 6 Hours of Onset (EXIT-BT2): a Prospective, Randomized, Open Label, Blinded Endpoint, and Multi-center Study

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
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 Unpublished pilot EXIT-BT (EXtending the tIme window of Thrombolysis by ButylphThalide up to 6 Hours after onset) suggest the safety, feasibility and potential benefit of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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥ 18 year

• Acute ischemic stroke confirmed by non-contrast computed tomography and use of CTA for assessment of LVO as determined by local investigators;

• The time from last known well to treatment: 4.5 - 6 hours;

• NIHSS ≥ 4 at randomization;

• First stroke onset or past stroke without obvious neurological deficit (mRS≤1);

• Uncertainty over the benefits and risks of thrombolysis by researcher;

• Signed informed consent.

Locations
Other Locations
China
Department of Neurology, General Hospital of Northern Theater Command
RECRUITING
Shenyang
Hui-Sheng Chen
RECRUITING
Shenyang
Time Frame
Start Date: 2024-02-01
Estimated Completion Date: 2026-12-15
Participants
Target number of participants: 1440
Treatments
Experimental: Tenecteplase group
intravenous thrombolysis with tenecteplase
Other: Control group
standard stroke care based on national guideline
Related Therapeutic Areas
Sponsors
Leads: General Hospital of Shenyang Military Region

This content was sourced from clinicaltrials.gov