Anesthesia Management in Endovascular Therapy for Ischemic Stroke (AMETIS)
Stroke, Thrombectomy, Anesthesia

About this trial
This is an interventional treatment trial for Stroke focused on measuring Anesthesia or Conscious sedation for Thrombectomy for Stroke, Thrombectomy, Anesthesia, Conscious sedation, Stroke
Eligibility Criteria
Inclusion Criteria:
- Acute anterior circulation ischemic stroke (terminal portion of the internal carotid artery, middle cerebral artery), with indication for radiological mechanical thrombectomy assessed by the neurology / neuroradiology team
- Over 18 years of age
- Benefiting from an affiliation to the French Social Security system
- Patient or familly informed consent. In case of patient incapacity and no family present, and due to the emergency of the procedure, the patient may be included on the sole decision of the investigator (emergency procedure with subsequent differed consent).
Exclusion Criteria:
- Altered vigilance defined by score ≥ 2 at item 1a "level of consciousness" of the NIHSS score
- Altered previous autonomy, defined by a modified Rankin score (mRS)> 1
- Acute ischemic stroke of posterior circulation or anterior cerebral artery
- Associated brain haemorrhage
- Pregnant or nursing women
- Patient under law protection
- Stroke complicating another acute illness or postoperative stroke.
Sites / Locations
- CHU de Clermont-Ferrand
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
General anaesthesia
Conscious Sedation
In the general anesthesia group, rapid sequence induction is used. Conduction of general anesthesia and drugs used are left to the expertise of each investigating center. Systolic blood pressure has to be maintained between 140 and 180 mmHg with an intravenous norepinephrine infusion if necessary, tele-expiratory carbon dioxyde concentration (EtCO2) has to be maintained between 30 and 35 mmHg and SpO2 has to be maintained between 94 and 98 %.
In the conscious sedation group, drugs choice as well as pharmacological modulation will be left to the expertise of each investigating center. A sedation level between 0 and -3 with spontaneous breathing will be targeted, using the Richmond Agitation Sedation Scale (RASS) score validated in French. The lightest sedation level will be targeted, i.e. minimal to moderate sedation according to the US recommendations for sedation / analgesia. Systolic blood pressure will be maintained between 140 and 180 mmHg with an intravenous norepinephrine infusion if necessary and SpO2 will be maintained between 94 and 98%.