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Anesthesia Management in Endovascular Therapy for Ischemic Stroke (AMETIS)

Primary Purpose

Stroke, Thrombectomy, Anesthesia

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
General anaesthesia
Conscious Sedation
Sponsored by
University Hospital, Clermont-Ferrand
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Active Comparator

Active Comparator

Arm Label

General anaesthesia

Conscious Sedation

Arm Description

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%.

Outcomes

Primary Outcome Measures

composite of functional independence at 3 months and absence of medical complication occurring by day 7 after endovascular therapy for anterior circulation AIS
The primary outcome measure is a composite of functional independence at 3 months and absence of medical complication occurring by day 7 after endovascular therapy for anterior circulation AIS. Functional independence is defined as a mRS score 0 to 2 by day 90. Medical complications are defined as intervention-associated arterial perforation or dissection, pneumonia or myocardial infarction or acute cardiogenic pulmonary oedema or malignant stroke evolution occurring by day 7

Secondary Outcome Measures

Ordinal score on the mRS by day 90
Functional independence by day 90 defined as a mRS score 0-2
Excellent recovery by day 90 defined as a mRS score 0-1
Moderate recovery by day 90 defined as a mRS score 0-3
Shift analysis of day 90 mRS adjusted for initial prognostic factors
(baseline mRS, age, initial NIHSS, carotid top occlusion)
Good recovery defined with sliding dichotomy responder analysis relating day 90 mRS with baseline NIHSS score: mRS 0 for NIHSS ≤ 7; mRS 0-1 for NIHSS 8-14; mRS 0-2 for NIHSS > 14
Intraprocedural hemodynamic and ventilatory conditions and complications defined as hypotension, blood pressure variability, hypoxemia and aspiration
Intervention-associated vessel and others complications defined as arterial dissection or perforation, groin hematoma, embolization in another arterial territory
Door to groin puncture delay
Door to reperfusion delay
Successful reperfusion defined by the modified Treatment In Cerebral Ischemia (mTICI) reperfusion scale of 2b or 3 (with a grade of 2b or 3 indicating reperfusion of > 50% of the affected territory)
NIHSS by day 1 and day 7
Stroke unit and hospital length of stay
Medical complications by day 7 defined as pneumonia, acute cardiogenic pulmonary oedema, myocardial infarction, extra pulmonary infection, venous thromboembolism, new event of AIS, epilepsy, gastrointestinal bleeding or other symptomatic bleeding
Malignant stroke evolution by day 7
Symptomatic intracranial haemorrhage by day 7 defined as brain haemorrhage on imaging associated with an increase of at least 4 points in the NIHSS score
Unexpected intensive care unit admission by day 7
Mortality by day 7 and day 90
Procedural feasibility score estimated by the radiologist and the anaesthesiologist and patient acceptability score

Full Information

First Posted
July 20, 2017
Last Updated
September 28, 2020
Sponsor
University Hospital, Clermont-Ferrand
Collaborators
Direction Générale de l'Offre de Soins
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1. Study Identification

Unique Protocol Identification Number
NCT03229148
Brief Title
Anesthesia Management in Endovascular Therapy for Ischemic Stroke
Acronym
AMETIS
Official Title
Anesthesia Management in Endovascular Therapy for Ischemic Stroke: A Multicenter Randomised Study
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
August 31, 2017 (Actual)
Primary Completion Date
May 13, 2020 (Actual)
Study Completion Date
June 30, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Clermont-Ferrand
Collaborators
Direction Générale de l'Offre de Soins

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Objective of the study: to assess whether pharmacological sedation or general anesthesia for treatment of anterior circulation ischemic stroke with endovascular mechanical thrombectomy is associated with difference in morbidity (neurological outcome and peri-procedural complications).
Detailed Description
Since 2015, the management of anterior acute ischemic stroke (AIS) involves endovascular treatment with mechanical thrombectomy (MT). This urgent, difficult and uncomfortable procedure in frail patients requires multidisciplinary care ideally involving neurologists, interventional neuroradiologists and anesthesiologists. Two anesthetic strategies are currently used: pharmacologic sedation in spontaneous ventilation or general anesthesia with tracheal intubation. General anesthesia provides strict immobility, protects the airway and avoids emergency intubation in case of severe procedural complication (notably vomiting and aspiration). Sedation is a frequently used alternative because of (1) a rapid execution which could reduce delay to reperfusion, (2) a lower risk of blood pressure drop that may compromise cerebral blood flow in the penumbra area, (3) the theoretical capacity to assess neurological status during the procedure and (4) the supposed risk of complications associated with mechanical ventilation and intravenous anesthestics on brain metabolism. Nevertheless, sedation exposes to dramatic complications in case of patient agitation and movements. The choice of the ideal anesthesic management is still lacking. Old retrospective studies seemed to favor sedation with worst neurological outcome associated with general anesthesia. Nevertheless, these datas suffered methodological issues with selection bias: more severe patients based on NIHSS score were rather treated with general anesthesia and blood pressure was not controlled. Recent studies that demonstrated the benefit of MT did not include a specific anesthetic protocol and none of the studies currently available included a blood pressure management protocol that appears to be an essential component of cerebral perfusion. A subgroup analysis of the MR Clean study, including patients with an identical initial NIHSS score, did not find benefit from MT in patients with general anesthesia compared to those receiving sedation. Finally, authors concluded that performing a MT under general anesthesia would significantly lengthen the reperfusion delay and nullify the benefit of MT. The prospective, randomized, single-center SIESTA trial, conducted in 150 patients with an anterior circulation AIS, found no difference in the early neurological improvement (primary endpoint), assessed on the change in NIHSS score between admission and the 24th hour, between the conscious sedation group and the general anesthesia group. There were a tendency for a better 3-month neurological outcome in the general anesthesia group (37% vs 18% of patients with a Modified Rankin score of 0-2 in the general anesthesia and conscious sedation groups respectively), but it was not possible to conclude due to a lack of statistical power. Due to the increasing number of patients eligible for endovascular MT and the potential implication of these two anesthetic management on the functional outcome, a study comparing general anesthesia and sedation during a MT seems essential as specified in the recent updated American Stroke Association guidelines. The objective of this study is to assess whether sedation or general anesthesia during endovascular treatment with mechanical thrombectomy is associated with a difference in morbidity (neurological outcome and peri-procedural complications), in anterior circulation AIS.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Thrombectomy, Anesthesia, Conscious Sedation
Keywords
Anesthesia or Conscious sedation for Thrombectomy for Stroke, Thrombectomy, Anesthesia, Conscious sedation, Stroke

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Multicentic, prospective, open, in parallel groups, stratified and randomised study.
Masking
Outcomes Assessor
Masking Description
It is an open label trial because it is not possible to maintain the anesthesiologist and patient blinded during the procedure. However, all subsequent evaluations will be conducted by clinical research staff blinded to the randomization group.
Allocation
Randomized
Enrollment
332 (Actual)

8. Arms, Groups, and Interventions

Arm Title
General anaesthesia
Arm Type
Active Comparator
Arm Description
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 %.
Arm Title
Conscious Sedation
Arm Type
Active Comparator
Arm Description
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%.
Intervention Type
Procedure
Intervention Name(s)
General anaesthesia
Intervention Description
Procedure in which patients are induced into an unconscious state through use of various medications so that they do not feel pain during surgery
Intervention Type
Procedure
Intervention Name(s)
Conscious Sedation
Intervention Description
A drug-induced depression of consciousness during which patients respond purposefully to verbal commands, either alone or accompanied by light tactile stimulation. No interventions are required to maintain a patent airway. (From: American Society of Anesthesiologists Practice Guidelines)
Primary Outcome Measure Information:
Title
composite of functional independence at 3 months and absence of medical complication occurring by day 7 after endovascular therapy for anterior circulation AIS
Description
The primary outcome measure is a composite of functional independence at 3 months and absence of medical complication occurring by day 7 after endovascular therapy for anterior circulation AIS. Functional independence is defined as a mRS score 0 to 2 by day 90. Medical complications are defined as intervention-associated arterial perforation or dissection, pneumonia or myocardial infarction or acute cardiogenic pulmonary oedema or malignant stroke evolution occurring by day 7
Time Frame
Day 90
Secondary Outcome Measure Information:
Title
Ordinal score on the mRS by day 90
Time Frame
at day 90
Title
Functional independence by day 90 defined as a mRS score 0-2
Time Frame
at day 90
Title
Excellent recovery by day 90 defined as a mRS score 0-1
Time Frame
at day 90
Title
Moderate recovery by day 90 defined as a mRS score 0-3
Time Frame
at day 90
Title
Shift analysis of day 90 mRS adjusted for initial prognostic factors
Description
(baseline mRS, age, initial NIHSS, carotid top occlusion)
Time Frame
at day 90
Title
Good recovery defined with sliding dichotomy responder analysis relating day 90 mRS with baseline NIHSS score: mRS 0 for NIHSS ≤ 7; mRS 0-1 for NIHSS 8-14; mRS 0-2 for NIHSS > 14
Time Frame
at day 90
Title
Intraprocedural hemodynamic and ventilatory conditions and complications defined as hypotension, blood pressure variability, hypoxemia and aspiration
Time Frame
at day 90
Title
Intervention-associated vessel and others complications defined as arterial dissection or perforation, groin hematoma, embolization in another arterial territory
Time Frame
at day 90
Title
Door to groin puncture delay
Time Frame
at day 90
Title
Door to reperfusion delay
Time Frame
at day 90
Title
Successful reperfusion defined by the modified Treatment In Cerebral Ischemia (mTICI) reperfusion scale of 2b or 3 (with a grade of 2b or 3 indicating reperfusion of > 50% of the affected territory)
Time Frame
at day 90
Title
NIHSS by day 1 and day 7
Time Frame
by day 1 and day 7
Title
Stroke unit and hospital length of stay
Time Frame
at day 90
Title
Medical complications by day 7 defined as pneumonia, acute cardiogenic pulmonary oedema, myocardial infarction, extra pulmonary infection, venous thromboembolism, new event of AIS, epilepsy, gastrointestinal bleeding or other symptomatic bleeding
Time Frame
at day 7
Title
Malignant stroke evolution by day 7
Time Frame
by day 7
Title
Symptomatic intracranial haemorrhage by day 7 defined as brain haemorrhage on imaging associated with an increase of at least 4 points in the NIHSS score
Time Frame
by day 7
Title
Unexpected intensive care unit admission by day 7
Time Frame
by day 7
Title
Mortality by day 7 and day 90
Time Frame
by day 7 and day 90
Title
Procedural feasibility score estimated by the radiologist and the anaesthesiologist and patient acceptability score
Time Frame
by day 7 and day 90

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Russel Chabanne, MD
Organizational Affiliation
CHU de Clermont-Ferrand
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU de Clermont-Ferrand
City
Clermont-Ferrand
State/Province
Auvergne
ZIP/Postal Code
63003
Country
France

12. IPD Sharing Statement

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Anesthesia Management in Endovascular Therapy for Ischemic Stroke

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