Why do some stroke patients not improve after clot removal? new study aims to find out
NCT ID NCT07534319
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at why about half of stroke patients don't recover well even after doctors successfully remove a blood clot from their brain. Researchers will use special MRI scans to measure blood flow changes in the brain at 3 days, 7 days, and 90 days after the procedure. They will follow 100 adult stroke patients to see if these blood flow patterns relate to how well patients recover 3 months later.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could help doctors identify why some stroke patients don't recover well after clot removal, potentially leading to better treatments.
- What could go wrong
- This is an early observational study with only 100 participants, so results may not apply to all patients. It aims to understand the problem, not test a new treatment.
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.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2025
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients with an acute ischemic stroke of the ICA, MCA or with tandem occlusion who have had a successful recanalization, defined as mTICI score ≥2b and with written informed consent of the patient or a family member
- Ages
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18 years and older
- 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: * Male and female subjects \>18 years old. * Acute ischemic stroke related to a new occlusion of the internal carotid artery, middle cerebral artery (M1- and/or M2-segment), or both. * Eligibility and performance of endovascular thrombectomy. * Achievement of successful recanalization, defined as mTICI score ≥2b * Written informed consent of the patient or when the patient is not able to participate in the consenting procedure, the written authorization of a family member. Foreign speaking patients should be included by a person with sufficient German language proficiency to act as a translator. Exclusion Criteria: * Documented evidence or a confirmed willingness of the patient not to participate in any scientific study. * Standard contraindications for MRI, such as pacemaker, metallic prothesis, glaucoma, metallic tattoo dyes, verbal confirmed pregnancy. Unwilling or unable to cooperate with breathing manoeuvres. * Major cardiopulmonary diseases, such as severe uncontrolled asthma bronchiale, severe chronic obstructive lung disease (i.e., GOLD stage ≥III), diffuse interstitial lung disease, pulmonary embolism, acute/subacute myocardial infarction, or severe heart failure (i.e., NYHA class ≥III). * Symptomatic increased intracranial pressure. * Presence of intracranial haemorrhage type ≥2 according to the Heidelberg classification. * New onset of seizure.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Zurich University Hospital
RECRUITINGZurich, Canton of Zurich, 8006, Switzerland
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Other studies related to the condition(s) this trial covers.
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