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A Multicenter, Retrospective, Observational Cohort Study on Intravenous Thrombolysis Beyond the Time Window for Acute Ischemic Stroke

A Multicenter, Retrospective, Observational Cohort Study on Intravenous Thrombolysis Beyond the Time Window for Acute Ischemic Stroke

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07419997
Acronym
TRAILBLAZER
Enrollment
2600
Registered
2026-02-19
Start date
2025-12-29
Completion date
2026-12-29
Last updated
2026-02-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Keywords

Acute ischemic stroke, Alteplase, Tenecteplase, Stroke at 4.5 to 24 Hours

Brief summary

A multicenter, retrospective, observational cohort study on intravenous thrombolysis beyond the time window for acute ischemic stroke

Interventions

None listed

Sponsors

Xuanwu Hospital, Beijing
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patients with acute ischemic stroke, regardless of gender; 2. Age ≥ 18 years old; 3. Time from onset to treatment within 4.5 - 24 hours (the onset time refers to the last time when they appeared normal); 4. Complete relevant clinical data (including gender, age, mRS, NIHSS, etc.).

Design outcomes

Primary

MeasureTime frameDescription
Proportion of study participants with mRS scores of 0 - 1at 90 (±7) daysProportion of study participants with mRS scores of 0 - 1

Secondary

MeasureTime frameDescription
Distribution of mRS scores ranging from 0 to 6at 90 (±7) daysDistribution of mRS scores ranging from 0 to 6
Proportion of study participants with mRS scores of 0 - 2at 90 (±7) daysProportion of study participants with mRS scores of 0 - 2
The proportion of study participants with a NIHSS score of ≤1 or a decrease of ≥8 points compared to the baselineat 24 (±12) hoursThe proportion of study participants with a NIHSS score of ≤1 or a decrease of ≥8 points compared to the baseline
mortality rateat 90 (±7) daysmortality rate
Symptomatic intracranial hemorrhagewithin 36 hoursSymptomatic intracranial hemorrhage

Countries

China

Contacts

CONTACTXin Xing, MD
drxingxin@126.com01083198082

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026