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Chilling the brain after stroke: new device tested in 8 patients

NCT ID NCT06634303

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

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

8 people

The number who actually took part.

Started

Jun 2025

Finished

Feb 2026

Lead sponsor

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

18 to 89 years

Sex

Anyone

Healthy volunteers

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

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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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

  • Vall d'Hebron University Hospital

    Barcelona, Spain

More trials for these conditions

Other studies related to the condition(s) this trial covers.