Observing treatment options for acute ischemic stroke in Southwest China
Official title: Registration of Acute Ischemic Stroke With Large and Medium-sized Vascular Occlusion in Southwest China(LMVOS)
Run by The Affiliated Hospital Of Southwest Medical University · NCT06125236 · Data updated 2026-11-12
This study is tracking 8,000 patients with acute ischemic stroke in Southwest China to see which treatment options work best and how they help people recover over 90 days.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 8000 (estimated) |
| Sponsor | The Affiliated Hospital Of Southwest Medical University Academic / other |
| Locations | 1 site (Luzhou) |
| Status | Recruiting |
| Started | November 9, 2023 |
| Main results expected | December 1, 2045 |
| Study ends | May 1, 2046 |
| Registry record updated | November 13, 2023 |
| Trial ID | NCT06125236 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are individuals diagnosed with acute ischemic stroke due to large or medium vessel occlusion.
✕Probably not a fit
Patients with acute ischemic stroke not caused by large or medium vessel occlusion may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to register and analyze treatment options for patients with acute ischemic stroke caused by large and medium-sized vascular occlusions. Over a period of 22 years, the study will enroll 8,000 patients to evaluate the safety and efficacy of various treatment strategies in real-world clinical settings. The study will follow patients and assess their outcomes at 90 days post-treatment, providing valuable insights into the management of this condition.
Why it matters
Potential benefit: If successful, this study could enhance understanding of effective treatment strategies for acute ischemic stroke, leading to improved patient outcomes.
How similar studies have gone: While this study is observational and focuses on real-world data, similar studies have shown success in understanding treatment outcomes for acute ischemic stroke.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: The clinical diagnosis is acute ischemic stroke with large- or medium- vessel occlusion (the criteria followed the Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke 2018). Informed consent from the patient or surrogate. Exclusion Criteria: No additional exclusion criteria.
Where it's running
-
Affiliated Hospital of Southwest Medical University
Luzhou, China Recruiting
Study contacts
- Study coordinator: Zhengzhou Yuan, MD
- Email: coneuro@163.com
- Phone: +868303165661
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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This trial tests whether a 5-day external trigeminal nerve stimulation given after stroke can help more patients recover better than a sham treatment.
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This phase II study tests whether LT3001 given to adults with acute ischemic stroke can help reopen blocked brain arteries.
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Mobilisation After Endovascular Stroke Treatment
This study checks whether moving around 12 hours after endovascular stroke treatment is as safe as moving around 24 hours for people with an acute ischemic stroke.
-
Endovascular therapy plus standard care vs standard care alone for distal and medium vessel strokes
In people with acute ischemic stroke due to distal or medium vessel blockages, this study tests whether adding endovascular treatment to the usual medical care helps improve outcomes compared with medical care alone.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.