Investigating cell-free DNA in acute stroke patients
Official title: CANTO - Cell-free DNA in Acute Stroke
Run by University Hospital, Basel, Switzerland · NCT06928675 · Data updated 2026-11-12
This study looks at how cell-free DNA in the blood of patients with a severe type of stroke can help us understand the cause of their stroke and how well they respond to treatment.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 200 (estimated) |
| Sponsor | University Hospital, Basel, Switzerland Academic / other |
| Locations | 1 site (Basel) |
| Status | Recruiting |
| Started | March 30, 2025 |
| Main results expected | September 1, 2026 |
| Study ends | September 1, 2026 |
| Registry record updated | April 15, 2025 |
| Trial ID | NCT06928675 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adults aged 18 and older who have experienced an acute ischemic stroke due to large vessel occlusion and require mechanical thrombectomy.
✕Probably not a fit
Patients currently undergoing immunological therapies, those with immunological diseases, or systemic infections at the time of admission 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 explore the role of cell-free DNA (cfDNA) in patients experiencing acute ischemic stroke due to large vessel occlusion. Researchers will analyze cfDNA in the hyperacute phase of stroke using blood and thrombus samples to understand its relationship with stroke etiologies, procedural factors like secondary embolization, and reperfusion outcomes. The study will also investigate the correlation between cfDNA content in blood and thrombus and identify the specific sources of cfDNA in different stroke subtypes.
Why it matters
Potential benefit: If successful, this study could enhance understanding of stroke mechanisms and improve treatment strategies for acute ischemic stroke.
How similar studies have gone: While the role of cfDNA in various conditions has been explored, this specific investigation in acute stroke is novel and has not been extensively tested in prior studies.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Acute ischemic stroke due to large vessel occlusion (LVO) who require mechanical thrombectomy (detected in CT-Scan or MRI-Scan) * 18 years of age Exclusion Criteria: * Patients currently undergoing immunological therapies. * Patients with immunological diseases * Patients with systemic infections at the time of admission
Where it's running
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University Hospital Basel
Basel, Switzerland Recruiting
Study contacts
- Principal investigator: Gerrit Grosse, PD Dr. Dr. — University Hospital, Basel, Switzerland
- Study coordinator: Gerrit Grosse, PD Dr. Dr.
- Email: gerrit.grosse@usb.ch
- Phone: +41 61 32 85265
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Deep phenotyping to explore recovery in young adults after stroke
This project will test whether a detailed health and sample-collection approach (deep phenotyping) is practical and acceptable for people aged 18–55 who have had a stroke.
-
Stem cell therapy for chronic stroke recovery
This study is testing whether using a patient's own stem cells can help people with long-term stroke recovery feel better and improve their daily functioning.
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AI-based tools to help diagnose, treat and predict stroke outcomes across multiple hospitals
This study tests AI-powered tools on real-world stroke patients to see if they can improve pre-hospital triage, diagnosis, and outcome prediction while data stay securely within each hospital.
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Web-based therapy using action observation and mirror therapy for arm weakness after stroke
This trial tests whether a mobile telerehabilitation app delivering action observation therapy (AOT) alone or combined AOT with mirror therapy (AOT-MT) can improve upper limb function in people with subacute stroke.
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Remote Ischaemic Conditioning for Fatigue After Stroke 2
Aat least 12 weeks after stroke, adults with post-stroke fatigue will try a simple hand-arm cuff treatment at home to see if it helps reduce fatigue.
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Dual-task balance training plus computer-based cognitive training after stroke
In adults who recently had a stroke, the study tests whether adding computerized cognitive exercises to balance training improves balance and other recovery outcomes.
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.