Ireland
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Recruiting Observational

Registration of Intravenous Thrombolysis for Acute Ischemic Stroke in Southwestern China(IVTIS)

NCT06131385 · tracked via the Priya Life Science China tracker
Sponsor
Zhengzhou Yuan
Phase
Observational
Started
2023-11-20
Last updated
2023-11-28

Condition(s) studied

Stroke, Acute

Investigational drug(s) / intervention(s)

intravenous thrombolysis

intravenous thrombolysis: Intravenous thrombolysis using thrombolytic drugs such as ateplase and teneplase.

Study summary

This study aims to observe the safety and effectiveness of intravenous thrombolysis for acute ischemic stroke in real-world clinical practice.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * The patient was diagnosed with acute ischemic stroke and received intravenous thrombolysis. Exclusion Criteria: * No additional exclusion criteria.

Primary outcome measure(s)

  • modified Rankin Scale (mRS) score — 90±7 days
    Ordinal distribution of mRS at 90±7 days; modified Rankin scale (range, 0 to 6, with a score of 0 indicating no disability, 1 no clinically significant disability, 2 slight disability, 3 moderate disability but remaining able to walk unassisted, 4 moderately severe disability, 5 severe disability, and 6 death)

Trial sites (1)

FacilityCityRegionStatus
Affiliated Hospital of Southwest Medical University Luzhou China Recruiting
Official registry record

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 NCT06131385 on ClinicalTrials.gov ↗ ← All trials in China