Biobank for patients with large vessel occlusion stroke
Official title: Cerebral Large Vessel Occlusion Stroke Multiomics Biosample Cohort
Run by First Affiliated Hospital of Wannan Medical College · NCT06963489 · Data updated 2026-11-12
This study is collecting blood and clot samples from patients with large vessel occlusion strokes to see if analyzing them can help improve diagnosis and treatment for these patients.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 500 (estimated) |
| Sponsor | First Affiliated Hospital of Wannan Medical College Academic / other |
| Locations | 5 sites (Wuhu, Anhui and 4 other locations) |
| Status | Recruiting |
| Started | April 27, 2025 |
| Main results expected | February 29, 2028 |
| Study ends | February 29, 2028 |
| Registry record updated | May 11, 2025 |
| Trial ID | NCT06963489 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adults over 18 years with confirmed large vessel occlusion ischemic stroke and available biological samples.
✕Probably not a fit
Patients who cannot provide biological samples or refuse to give informed consent will 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 multicenter, ambispective cohort study collects and analyzes blood and thrombus samples from patients with acute ischemic stroke caused by large vessel occlusion. The study aims to establish a comprehensive multiomics biobank, which includes clinical, laboratory, imaging, and follow-up data from five stroke centers. By performing detailed analyses such as metabolomics, proteomics, and genomics, researchers seek to identify phenotypic differences and develop clinical prediction models to improve diagnosis and prognosis for these patients. The rich dataset will also facilitate further scientific inquiries related to stroke.
Why it matters
Potential benefit: If successful, this study could lead to improved diagnostic and prognostic tools for patients suffering from large vessel occlusion strokes.
How similar studies have gone: Other studies utilizing multiomics approaches have shown promise in understanding complex conditions, suggesting potential success for this novel approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Age over 18 years. 2. Patients with intracranial and extracranial large vessel occlusion ischemic stroke confirmed by cerebrovascular angiography. 3. Availability of complete clinical and follow-up information required for the study. 4. Availability of blood and/or thrombus biological samples. 5. Voluntary written informed consent signed by the patient or their family (1) For retrospectively enrolled patients, a "broad informed consent" was signed at the time of sample collection. Upon enrollment into the cohort, a follow-up phone call was made to confirm the informed consent. (2) For prospectively enrolled patients, informed consent for this study was signed at the time of enrollment by the patient or their family. Exclusion Criteria: 1. Patients for whom biological samples cannot be obtained; 2. Patients or their family members who refuse to sign the informed consent form.
Where it's running
-
Baotou Central Hospital
Baotou, Inner Mongolia, China Recruiting -
Affiliated Hospital of Shandong University of Traditional Chinese Medicine Hospital
Jinan, Shandong, China Recruiting -
The First Affiliated Hospital of zhengzhou University
Henan, Zhengzhou, China Recruiting -
Capital medical university of Beijing Tiantan Hospital
Beijing, China Recruiting -
The First Affiliated Hospital of Shihezi University
Wuhu, Anhui, China Not yet recruiting
Study contacts
- Study coordinator: Zhiyuan Feng, MD
- Email: fzyhhz1996@gmail.com
- Phone: 86+15801290121
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Sevoflurane vs. Propofol for anesthesia in stroke patients undergoing clot-removal
This study tests whether sevoflurane or propofol used for anesthesia during endovascular treatment of an acute ischemic stroke affects the final brain damage and recovery.
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Tenecteplase or Reteplase Bridging Before Thrombectomy in Acute Ischemic Stroke
This trial tests whether giving tenecteplase or reteplase before mechanical thrombectomy helps people with acute ischemic stroke due to large vessel occlusion, compared with doing thrombectomy alone.
-
Sivelestat added to endovascular clot retrieval for acute anterior circulation stroke
This study tests whether giving sivelestat sodium alongside mechanical thrombectomy helps improve outcomes for adults with acute ischemic stroke due to large vessel occlusion.
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Non-invasive vagus nerve stimulation to lower inflammation and brain injury markers after acute ischemic stroke
This test tries whether adding non-invasive vagus nerve stimulation to usual care lowers inflammation and blood markers of brain injury in adults with acute ischemic stroke from a large vessel occlusion.
-
Tenecteplase before transfer for anterior circulation large-vessel stroke (4.5–24 hours)
This will test whether a single bolus of tenecteplase given at the first hospital before transfer helps people with anterior circulation large-vessel ischemic stroke who present 4.5–24 hours after they were last well.
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CONDA stent retriever for reopening large-vessel blockages in acute ischemic stroke.
The CONDA stent retriever will be tried to reopen blocked large brain arteries in adults with acute ischemic stroke treated within 24 hours of symptom onset.
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.