Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT06530927

Microclots and Neutrophil Activation as Potential Indicators for Stroke Risk and Reperfusion Failure

Led by University of Zurich · Updated on 2025-08-29

500

Participants Needed

1

Research Sites

304 weeks

Total Duration

On this page

Sponsors

U

University of Zurich

Lead Sponsor

E

Empa, Swiss Federal Laboratories for Materials Science and Technology

Collaborating Sponsor

AI-Summary

What this Trial Is About

Stroke remains a major health burden worldwide. Many patients are severely disabled and stay in need of care. Mechanical thrombectomy has dramatically improved outcomes for stroke patients with large vessel occlusions, yet 40-50% of patients with successful recanalization remain severely disabled despite successful recanalization, a scenario called "futile recanalization". One of the causes for this lack of treatment effect is capillary obstruction, or "no reflow", potentially resulting from activated neutrophils and micrometer-sized blood clots. To address this issue, we employ digital holotomographic and atomic force microscopy to investigate the structural and chemical characteristics of blood and clot material in stroke patients and individuals at high risk of developing a stroke. Our study elucidates the association of activated neutrophils and microclots with stroke risk, and may be associated with clinical outcome, stroke ethology and reperfusion failure in patients with stroke. Leveraging label-free microscopy tools, could potentially lead to the discovery of new biomarkers for individualized stroke treatment and prevention, ultimately offering rapid identification of at risk patients and improving clinical outcomes

CONDITIONS

Official Title

Microclots and Neutrophil Activation as Potential Indicators for Stroke Risk and Reperfusion Failure

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients without acute stroke or with previous stroke at least 1 year ago
  • Signed informed consent
  • Patients admitted with high suspicion of acute ischemic stroke
  • Stroke symptoms started within 12 hours
  • Consent according to emergency research regulations
  • Ischemic stroke confirmed later
Not Eligible

You will not qualify if you...

  • Pregnancy
  • Age under 18 years
  • Acute stroke no therapy group: acute treatment with IVT or MT
  • Acute stroke IVT group: acute treatment with MT or without IVT
  • Acute stroke MT group: acute treatment without MT

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Hospital Zurich

Zurich, Canton of Zurich, Switzerland, 8091

Actively Recruiting

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Research Team

L

Lukas Otto, Dr. med.

CONTACT

S

Susanne Wegener, Prof.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

5

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