Could unclogging brain arteries prevent strokes?
NCT ID NCT07699003
First seen Jul 13, 2026 · Last updated Jul 14, 2026 · Updated 1 time
Summary
This trial compares a procedure to reopen blocked brain arteries (using balloons and stents) against standard medical therapy in people with chronic blockages. The goal is to see if the procedure reduces the risk of stroke or death within a year. Participants have had symptoms from the blockage for at least four weeks and are otherwise relatively healthy.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Endovascular recanalization (balloon angioplasty and/or stent implantation)
- What this could lead to
- If successful, this procedure could offer a new way to lower stroke risk in people with long-standing blockages in brain arteries, potentially improving outcomes beyond standard medication.
- What could go wrong
- The procedure carries risks like stroke, bleeding, or vessel damage. This is a randomized trial, so results may show no benefit over medication alone, and findings may not apply to all patients.
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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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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About 382 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 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 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: 1. Age ≥18 years 2. Occlusion of the unilateral middle cerebral artery, basilar artery, intracranial internal carotid artery, or vertebral artery, as confirmed by computed tomography angiography (CTA), magnetic resonance angiography (MRA), or digital subtraction angiography (DSA) 3. Modified Rankin Scale (mRS) score of 0-2 4. Presence of symptoms related to the occluded vessel, as determined by the physician, with the most recent symptom onset occurring more than 4 weeks and within 6 months prior to enrolment 5. The subject or their legally authorised representative has provided written informed consent for the study Exclusion Criteria: 1. Evidence of hemorrhage on CT or MRI 2. Large hemispheric infarction involving \>50% of the middle cerebral artery territory on CT or MRI 3. Severe pre-stroke disability (modified Rankin Scale score ≥2) or life expectancy \<12 months 4. Major comorbidities that may interfere with outcome assessment and follow-up (e.g., severe heart failure, renal failure, etc.) 5. Uncontrolled seizure at the time of stroke onset 6. Baseline platelet count \<50,000/μL 7. Severe, persistent hypertension that remains uncontrolled despite active management (systolic blood pressure \>220 mmHg or diastolic blood pressure \>120 mmHg) 8. Known inherited or acquired bleeding diathesis, coagulation factor deficiency, or recent oral anticoagulant therapy with an international normalized ratio (INR) \>3 9. Suspected septic emboli or suspected bacterial endocarditis 10. Known allergy to iodine, heparin, or anaesthetics, or other definite contraindications to endovascular procedures 11. Pregnant women 12. Other severe, progressive, or terminal diseases (as judged by the investigator), or life expectancy \<24 months 13. Prior attempted endovascular recanalization therapy before randomization 14. Current participation in other studies involving investigational drugs or devices 15. Evidence of intracranial tumour on CT or MRI (except meningioma) 16. Excessive tortuosity of cervical vessels on CTA/MRA that may preclude endovascular therapy
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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.