Chilling the brain after stroke: new device tested in 8 patients
NCT ID NCT06634303
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This early study tested a new device that cools the brain in 8 people who had a stroke caused by a large blood clot. After doctors removed the clot, the device cooled the brain for 30 minutes to try to protect it from further damage. The main goal was to see if the cooling was safe and worked as intended.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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8 people
The number who actually took part.
- Started
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Jun 2025
- Finished
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Feb 2026
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 89 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age 18 to 89 2. Informed signed consent obtained from patient or legally authorized representative 3. Clinical symptoms consistent with acute ischemic stroke 4. Pre-stroke modified Rankin Scale (mRS) score 0-1 5. National Institute of Health Stroke Scale (NIHSS) ≥ 6 6. Alberta Stroke Program Early CT Score (ASPECTS) score 5-10 7. IV tissue plasminogen activator (tPA) or Tenecteplase (TNK) may be administered within 4.5h of last known well (LKW), if patient eligible 8. Mechanical thrombectomy (MT) treatment performed with arterial puncture within 24h of LKW. 9. Pre-MT catheter angiogram shows target occlusion in intracranial ICA, M1 MCA, or M2 MCA 10. End of MT catheter angiogram shows achievement of moderate-to-complete reperfusion (modified Treatment in Cerebral Ischemia score or mTICI 2a-3) Exclusion Criteria: 1. Pre-MT CT or MRI shows acute intracranial hemorrhage. 2. Previous intracranial hemorrhage, AVM, neoplasm (except small meningioma), or vascular stent-implant 3. Coma or reduced level of consciousness prior to MT (NIHSS 1A\>1) 4. Seizure between LKW and time of potential enrollment 5. Severe contrast allergy or absolute contraindication to iodinated contrast. 6. Hypersensitivity to cold, i.e., history of cold-sensitive antibodies, Raynaud syndrome, or hepatitis C 7. Hematocrit \<33% 8. Severe known renal impairment, i.e., requires renal replacement therapy (dialysis). 9. Post-reperfusion investigational therapy cannot be started within 150 min following pre-treatment CT or MR imaging 10. Presumed septic embolism, suspicion of bacterial endocarditis. 11. Known pregnancy (in women with child-bearing potential) 12. Body weight \< 40kg 13. Patient not willing and able to participate in follow-up visits to day 90. 14. Life expectancy \<6 months due to pre-existing conditions such as severe heart or renal failure, cancer, etc. 15. Currently or within past 30 days participating in another investigational treatment study
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Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Vall d'Hebron University Hospital
Barcelona, Spain
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Other studies related to the condition(s) this trial covers.
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