Micro-clots and Neutrophil Activation as Potential Indicators for Stroke Risk and Reperfusion Failure The CLOTSAFE - Study (Micro-CLOTs, Stroke Risk, Activated Neutrophils, Reperfusion FailurE)

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

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

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

⁃ Patients without acute stroke CS or CSG

• No previous stroke or previous stroke ≥ 1 year ago

• Signed informed consent

⁃ Patients with acute stroke (AS-noTx, AS-IVT, AS-MT):

• Patients admitted with high suspicion of acute ischemic stroke

• Time of onset of stroke symptoms ≤ 12 hours

• Consent according to the regulations of research in an emergency situation

• Ischemic stroke later confirmed

Locations
Other Locations
Switzerland
University Hospital Zurich
RECRUITING
Zurich
Contact Information
Primary
Lukas Otto, Dr. med.
lukasbastian.otto@usz.ch
+41 43 253 13 01
Backup
Susanne Wegener, Prof.
susanne.wegener@usz.ch
+41 44 255 10 78
Time Frame
Start Date: 2025-02-01
Estimated Completion Date: 2030-12-01
Participants
Target number of participants: 500
Treatments
Control Group
Patients without previous documented stroke
Chronic Stroke Group
Patients with previous stroke ≥1year ago
Acute Stroke No Therapy Group
Patients with acute stroke, but without intravenous thrombolysis or mechanical thrombectomy
Acute Stroke IVT only Group
Patients with acute stroke and intravenous thrombolysis
Acute Stroke MT-Group
Patients with acute stroke and mechanical thrombectomy
Related Therapeutic Areas
Sponsors
Collaborators: Empa, Swiss Federal Laboratories for Materials Science and Technology
Leads: University of Zurich

This content was sourced from clinicaltrials.gov