Clinical trial Recruiting at 4 sites Observational

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 typeObservational
SexAll
Enrollment500 (estimated)
SponsorFirst Affiliated Hospital of Wannan Medical College
Academic / other
Locations5 sites (Wuhu, Anhui and 4 other locations)
StatusRecruiting
StartedApril 27, 2025
Main results expectedFebruary 29, 2028
Study endsFebruary 29, 2028
Registry record updatedMay 11, 2025
Trial IDNCT06963489 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

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.