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Clinical Trials in China / NCT06633809
Recruiting Observational

Therapy Evaluation in Patients With Minor Stroke and Large Vessel Occlusion

NCT06633809 · tracked via the Priya Life Science China tracker
Sponsor
Sir Run Run Shaw Hospital
Phase
Observational
Started
2021-11-22
Last updated
2024-10-09

Condition(s) studied

Stroke, AcuteCerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesVascular DiseasesBrain InfarctionNervous System Diseases

Investigational drug(s) / intervention(s)

Immediate endovascular therapy

Immediate endovascular therapy: The best medical therapy includes intravenous fibrinolysis, anticoagulants or antiplatelet, but NOT any immediate endovascular therapies.

Study summary

This multicenter registry study, which record the therapy strategy and follows up these acute ischemic stroke (AIS) patients with low NIHSS and large vessel occlusion (LVO), is intended to provide the important data for therapy evaluation and prognostic prediction of the LVO patients with low NIHSS.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: 1. Aged 18 years or older 2. Acute ischemic stroke patients of NIHSS 0-5 with 24 hours after onset 3. Proximal intracranial artery occlusion on NCCT/CTA or MRI/MRA showing occlusion of the intracranial ICA, M1, or proximal M2 vessel 4. Baseline ASPECTS ≥6 or infarct Core Volume of \< 70 on NCCT/DWI/CTP 5. Pre-mRS≤1 Exclusion Criteria: 1. Any sign of intracranial hemorrhage on baseline CT/MR; 2. Seizures at stroke onset 3. Baseline blood glucose of \<2.78 mmol or \>22.20 mmol, or platelet count \< 100,000/uL or serum creatinine levels \> 3.0 mg/dL 4. Participation in any investigational study in the previous 30 days

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Sir Run Run Shaw Hospital Hangzhou Zhejiang Recruiting

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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 NCT06633809 on ClinicalTrials.gov ↗ ← All trials in China