Clinical Trials in China / NCT06131385
Recruiting
Observational
Registration of Intravenous Thrombolysis for Acute Ischemic Stroke in Southwestern China(IVTIS)
NCT06131385 · tracked via the Priya Life Science China tracker
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| Affiliated Hospital of Southwest Medical University | Luzhou | China | Recruiting |
More Zhengzhou Yuan trials in China
Other trials for the same condition
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