Can a drug boost brain recovery after stroke?
NCT ID NCT06339411
First seen Aug 10, 2026 · Last updated Aug 12, 2026 · Updated 2 times
Summary
This trial tests whether Cerebrolysin, given after a procedure to remove a blood clot from the brain, can reduce tissue damage and improve recovery in people with acute ischemic stroke. The study involves 100 adults aged 18 to 80 who undergo successful clot removal within 6 to 24 hours of stroke onset. Participants receive either Cerebrolysin or a placebo infusion daily for 10 days, and researchers measure brain injury on MRI and track functional recovery over a year.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Cerebrolysin, a drug given by intravenous infusion for 10 days after stroke clot removal
- What this could lead to
- If it works, Cerebrolysin could reduce brain damage and improve recovery after stroke, potentially leading to a new standard of care.
- What could go wrong
- This is an early-phase trial with a modest number of participants, so results may not be conclusive. There is also a risk of side effects like bleeding in the brain.
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
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2030
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.
- Ages
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18 to 80 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: * Age 18 to 80 years. * Acute anterior-circulation ischemic stroke caused by internal carotid artery or M1 or M2 middle cerebral artery occlusion confirmed by computed tomography angiography. * Stroke onset-to-groin-puncture interval greater than 6 hours and no more than 24 hours. * Prestroke modified Rankin Scale score of 0 to 2. * Baseline National Institutes of Health Stroke Scale score of at least 6 with cortical signs. * Alberta Stroke Program Early Computed Tomography Score greater than 3. * Computed tomography perfusion target mismatch defined as ischemic core volume less than 70 mL, mismatch ratio at least 1.8, and mismatch volume at least 15 mL. * Moderate-to-good collateral circulation, defined as filling of more than 50% of the middle cerebral artery territory on computed tomography angiography. * Successful endovascular reperfusion, defined as modified Thrombolysis in Cerebral Infarction grade 2b or 3, confirmed before randomization. * Study treatment can be initiated within 36 hours of stroke onset. * Written informed consent obtained before randomization from the participant or a legally authorized representative. Exclusion Criteria: * Life expectancy less than 6 months or a serious medical, neurological, or psychiatric condition likely to interfere with study treatment, follow-up, or outcome assessment. * Current pregnancy or breastfeeding. * Known iodinated contrast allergy that precludes required endovascular or imaging procedures. * Acute or chronic renal failure with creatinine clearance less than 30 mL/min. * Known hypersensitivity or contraindication to Cerebrolysin. * Aspartate aminotransferase or alanine aminotransferase greater than 2 times the upper limit of normal, or total bilirubin greater than 2 mg/dL. * Blood glucose less than 50 mg/dL or greater than 400 mg/dL. * Platelet count less than 50,000/mm3 or international normalized ratio greater than 3. * Seizure at stroke onset that prevents reliable neurological assessment. * Pre-existing intracranial hemorrhage or multiple vascular occlusions on baseline neuroimaging.
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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 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.
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