Single-Patient trial gauges new stroke tool
NCT ID NCT02971826
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at how well the ReVive™ SE device works to restore blood flow in the brain during a stroke. Only one patient took part, and the goal was to see if the device is useful in standard care. The main measure was how much blood flow returned after using the device.
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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1 person
The number who actually took part.
- Started
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Nov 2018
- Finished
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Jun 2019
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient with an ischemic stroke detected by Computed Tomography (CT) or Magnetic Resonance Image (MRI) * Large proximal arterial occlusion : M1 segment of the Middle cerebral artery (MCA), Internal Carotid Artery (ICA) or Basilar Artery (BA) * Last known well (without neurological symptoms) ≤ 8 hours of treatment initiation * Score NIHSS ≥4 * Eligibility on an endovascular procedure using REVIVETM SE device * No opposition of the patient to participate at the study Exclusion Criteria: * Diagnostic cerebral imaging impossible * Distal occlusion * Tortuous vessel or other specificity preventing the access of device * Vessel diameter \< 1.5 mm * Known hypersensibility or allergy to nitinol * Subjects not covered by or having the right to social security * Deprivation of civil rights (guardianship, safeguard justice)
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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
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Hospices Civils de Lyon - Neuroradiology unit
Bron, 69500, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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