Systemic Inflammation During Recanalization of Cerebral Arterial Occlusion
NCT ID: NCT04731584
Last Updated: 2023-02-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
15 participants
OBSERVATIONAL
2021-04-07
2021-06-12
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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AVC
Patients hospitalized for TM after a proximal ischemic stroke of the middle cerebral artery and whose reperfusion is satisfactory (TICI 2b, 2c and 3). Additional blood sample will be taken during usual treatment the day of the stroke.
Blood sample
Patients from 2 groups will undergo blood sample (during a blood sample for there care) and inflammation parameters will be measure the day of the stroke
Control
Population of control patients, consisting of patients admitted on an outpatient basis for a diagnostic cerebral arteriography.
Blood sample
Patients from 2 groups will undergo blood sample (during a blood sample for there care) and inflammation parameters will be measure the day of the stroke
Interventions
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Blood sample
Patients from 2 groups will undergo blood sample (during a blood sample for there care) and inflammation parameters will be measure the day of the stroke
Eligibility Criteria
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Inclusion Criteria
* Ischemic stroke by occlusion of a middle cerebral artery (proximal portion M1)
* Initial diagnostic MRI infusion
* TM with complete reperfusion (TICI 2b, 2c or 3)
* TM performed under local anesthesia +/- anxiolysis, or sedation including propofol
* mRS prior to stroke \<2
* Barthel index \<90
* Included in the HIBISCUS cohort
* Patient who was informed and did not object to participating in the study OR included through the emergency procedure then collection of his non-objection or that of his trusted person as soon as possible
* Adults patient (s)
* mRS \<2
* Barthel index \<90
* Requiring diagnostic arteriography for routine check-up of a cerebrovascular malformation
* Patient who was informed and did not object to participating in the study
Exclusion Criteria
* Haemorrhagic complication before thrombectomy
* Pregnant woman
* Multiple vascular occlusions
* Occlusions of posterior or anterior cerebral territories other than M1
* Protected major
* TM performed under general anesthesia
* Other vital failure than neurological failure
GROUP "CONTROL" :
* NIHSS awareness score\> or = 2
* Pregnant woman
* Protected major
* Exam performed under general anesthesia
18 Years
ALL
No
Sponsors
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Hospices Civils de Lyon
OTHER
Responsible Party
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Locations
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Service d'Anesthésie Réanimation Hôpital - Neurologique/Groupement Est
Bron, , France
Service de Neurologie vasculaire - Hôpital Neurologique/Groupement Est
Bron, , France
Service de Neuroradiologie interventionnelle - Hôpital Neurologique/Groupement Est
Bron, , France
Service d'Anesthésie Réanimation - Hôpital Edouard Herriot/Groupement Centre
Lyon, , France
Countries
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Other Identifiers
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69HCL20_1080
Identifier Type: -
Identifier Source: org_study_id
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