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Randomization of Endovascular Treatment in Acute Ischemic Stroke in the Extended Time Window (RESILIENTExt)

Primary Purpose

Stroke, Ischemic

Status
Unknown status
Phase
Phase 3
Locations
Brazil
Study Type
Interventional
Intervention
Thrombectomy
Sponsored by
Hospital de Clinicas de Porto Alegre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke, Ischemic focused on measuring stroke, ischemic stroke, thrombectomy, treatment, acute stroke

Eligibility Criteria

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

Inclusion Criteria:

  1. Acute ischemic stroke where patient is ineligible for IV thrombolytic treatment or the treatment is contraindicated (e.g., subject presents beyond recommended time from symptom onset), or where patient has received IV thrombolytic therapy without clinical improvement.
  2. No significant pre-stroke functional disability (mRS ≤2)
  3. Baseline NIHSS score obtained prior to randomization must be equal or higher than 8 points (assessed within one hour prior to qualifying imaging)
  4. Age ≥18 years (no upper age limit)
  5. Occlusion (TICI 0-1) of the intracranial ICA (distal ICA or T occlusions) and/or MCA-M1 segment suitable for endovascular treatment, as evidenced by CTA, MRA or angiogram, with or without concomitant cervical carotid occlusion or stenosis.
  6. The presence of Age-Adjusted modified Clinical ASPECTS Mismatch (mCAM) defined as ASPECTS 5-10 and one of the following criteria:

    1. NIHSS ≥ 8 and >50% involvement in 0-1 Cortical (e.g. M1-6) ASPECTS areas (any age);
    2. NIHSS ≥ 8 and >50% involvement in 0-2 Cortical (e.g. M1-6) ASPECTS areas (and age < 80 years old);
    3. NIHSS ≥ 15 and >50% involvement in 0-3 Cortical (e.g. M1-6) ASPECTS areas (and age < 80 years old).
  7. Patient treatable within 6-24 hours of symptom onset. Symptoms onset is defined as point in time the patient was last seen well (at baseline). Treatment start is defined as arterial puncture.
  8. Informed consent obtained from patient or acceptable patient surrogate

Exclusion Criteria:

-Clinical criteria

  1. Known hemorrhagic diathesis, coagulation factor deficiency, or oral anticoagulant therapy with INR > 3.0
  2. Baseline platelet count < 30.000/µL
  3. Baseline blood glucose of < 50mg/dL
  4. Severe, sustained hypertension (SBP > 185 mm Hg or DBP > 110 mm Hg) NOTE: If the blood pressure can be successfully reduced and maintained at the acceptable level using AHA guidelines recommended medication (including iv antihypertensive drips), the patient can be enrolled.
  5. Patients in coma defined as totally unresponsive; responding only with reflexes or being areflexic (Intubated patients for transfer could be randomized only in case an NIHSS is obtained by a neurologist prior transportation).
  6. Seizures at stroke onset which would preclude obtaining a baseline NIHSS
  7. Serious, advanced, or terminal illness with anticipated life expectancy of less than one year.
  8. History of life-threatening allergy (more than rash) to contrast medium
  9. Subjects who has received IV t-PA treatment beyond 4.5 hours from the beginning of the symptoms
  10. Woman of childbearing potential who is known to be pregnant or who has a positive pregnancy test on admission.
  11. Subject participating in a study involving an investigational drug or device that would impact this study.
  12. Cerebral vasculitis
  13. Patients with a pre-existing neurological or psychiatric disease that would confound the neurological or functional evaluations, mRS score at baseline must be ≤2. This excludes patients who are severely demented, require constant assistance in a nursing home type setting or who live at home but are not fully independent in activities of daily living (toileting, dressing, eating, cooking and preparing meals, etc.)
  14. Unlikely to be available for 90-day follow-up (e.g. no fixed home address, visitor from overseas).

    - Neuroimaging criteria

  15. Hypodensity on CT or restricted diffusion on MRI amounting to an ASPECTS score of <5.
  16. Complete involvement of more than 3 cortical ASPECTS areas (e.g. M1, M2, M3, M4, M5, or M6).
  17. Complete absence of leptomeningeal collaterals on CT angiography (e.g. Malignant CTA pattern or score 0).
  18. CT or MR evidence of hemorrhage (the presence of GRE microbleeds is allowed).
  19. Significant mass effect with midline shift.
  20. Evidence of ipsilateral carotid occlusion, high grade stenosis or arterial dissection in the extracranial or petrous segment of the internal carotid artery that cannot be treated or will prevent access to the intracranial clot or excessive tortuosity of cervical vessels precluding device delivery/deployment
  21. Subjects with occlusions in multiple vascular territories (e.g., bilateral anterior circulation, or anterior/posterior circulation)
  22. Evidence of intracranial tumor (except small meningioma).

Sites / Locations

  • Hospital Geral de FortalezaRecruiting
  • Hospital de BaseRecruiting
  • Associacao Congregacao de Santa CatarinaRecruiting
  • Hospital das Clínicas de UberlândiaRecruiting
  • Hospital de Clínicas da Universidade Federal do Paraná
  • Conferencia Sao jose do Avai
  • Hospital de Clinicas de Porto AlegreRecruiting
  • Irmandade da Santa Casa de Misericordia de Porto Alegre - ISCMPA
  • Hospital das Clínicas da Faculdade de Medicina de Botucatu
  • Hospital de Clínicas - UNICAMP
  • Hospital das Clinicas de Ribeirao PretoRecruiting
  • Fundacao Faculdade Regional de Medicina S J Rio Preto
  • Instituto de Assistência Médica ao Servidor Público Estadual de Sao Paulo
  • Universidade Federal de São Paulo - UNIFESP/EPM

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

thrombectomy

Clinical treatment

Arm Description

mechanical thrombectomy with stent-retriever and/or thromboaspiration

Best Medical treatment

Outcomes

Primary Outcome Measures

Modified Rankin Scale scores
Distribution of the modified Rankin Scale scores at 90 days (shift analysis). The score range from zero to 6 with higher values indicating a worst functional outcome at 90 days

Secondary Outcome Measures

Proportion of Patients with Functional independence in 90 days
Functional independence defined as mRS ≤2
Disability on the utility-weighted modified Rankin scale (UW-mRS)
Mean score for disability on the utility-weighted modified Rankin scale (UW-mRS). The score range from 1 to zero with higher values indicating a better functional outcome at 90 days
Quality of life measured by EuroQol Group 5-Dimension Self-Report Questionnaire (EuroQol / EQ5D)
Quality of life analysis as measured by EuroQol/EQ5D 5-Dimension Self-Report Questionnaire, on which scores range from -0.176 to 1, with higher values indicating a better quality of life]) at 90 days
Mortality at 90 days
Mortality at 90 days
Proportion of patients with Intracranial Hemorrhage at 24 hours
Clinically significant ICH rates at 24 (-2/+12) hours. All intracerebral hemorrhages will be classified by a central core-lab using the Heidelberg criteria. Symptomatic ICH will be defined as per the SITS-MOST definition: deterioration in NIHSS score of ≥4 points within 24 hours from treatment and evidence of intraparenchymal hemorrhage type 2 in the 22 to 36 hours follow-up imaging scans.
Procedural related complications
Procedural related complications: arterial perforation, arterial dissection, and embolization in a previously uninvolved vascular territory

Full Information

First Posted
February 3, 2020
Last Updated
February 7, 2021
Sponsor
Hospital de Clinicas de Porto Alegre
Collaborators
Hospital das Clínicas de Ribeirão Preto, Hospital Geral de Fortaleza, Hospital de Base, Federal University of São Paulo, Fundação Faculdade Regional de Medicina de São José do Rio Preto, UPECLIN HC FM Botucatu Unesp, University of Campinas, Brazil, Irmandade Santa Casa de Misericórdia de Porto Alegre, Universidade Federal do Paraná, Hospital Estadual Central, Hospital Sao Jose do Avai, Irmandade da Santa Casa de Misericordia de Sao Paulo, Federal University of Uberlandia, Instituto de Assistencia Medica ao Servidor Publico Estadual, Sao Paulo
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1. Study Identification

Unique Protocol Identification Number
NCT04256096
Brief Title
Randomization of Endovascular Treatment in Acute Ischemic Stroke in the Extended Time Window
Acronym
RESILIENTExt
Official Title
Randomization of Endovascular Treatment With Stent-retriever and/or Thromboaspiration vs. Best Medical Therapy in Acute Ischemic Stroke Due to Large VEssel OcclusioN Trial in the Extended Time Window
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Unknown status
Study Start Date
March 9, 2020 (Actual)
Primary Completion Date
February 1, 2022 (Anticipated)
Study Completion Date
May 1, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital de Clinicas de Porto Alegre
Collaborators
Hospital das Clínicas de Ribeirão Preto, Hospital Geral de Fortaleza, Hospital de Base, Federal University of São Paulo, Fundação Faculdade Regional de Medicina de São José do Rio Preto, UPECLIN HC FM Botucatu Unesp, University of Campinas, Brazil, Irmandade Santa Casa de Misericórdia de Porto Alegre, Universidade Federal do Paraná, Hospital Estadual Central, Hospital Sao Jose do Avai, Irmandade da Santa Casa de Misericordia de Sao Paulo, Federal University of Uberlandia, Instituto de Assistencia Medica ao Servidor Publico Estadual, Sao Paulo

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
A phase III, randomized, multi-center, open label clinical trial that will examine whether endovascular treatment is superior to standard medical therapy alone in patients who suffer a large vessel anterior circulation ischemic stroke within 8-24 hours from time last seen well
Detailed Description
Prospective, multi-center, randomized, controlled, open-label, blinded-endpoint trial with a sequential design. The randomization employs a 1:1 ratio of mechanical thrombectomy with stent-retriever and/or thromboaspiration versus medical management alone in patients who suffer a large vessel anterior circulation ischemic stroke between 8 and 24 hours from time last seen well. Randomization will be done under a minimization process using age (≤68 vs. >68 years), baseline NIHSS (<17 v. ≥17), ASPECTS (5-7 vs. 8-10), therapeutic window (6-12 or 12-24 hours after TLKW), occlusion site (Intracranial ICA or M1), and clinical site. For the primary endpoint, subjects will be followed for 90 days post-randomization. Sham endovascular procedure has been rejected due to the medical risk of the angiography and practical issues that difficult to maintain blindness of investigators.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Ischemic
Keywords
stroke, ischemic stroke, thrombectomy, treatment, acute stroke

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
The randomization employs a 1:1 ratio of mechanical thrombectomy with stent-retriever and/or thromboaspiration versus medical management alone
Masking
Outcomes Assessor
Masking Description
Sham endovascular procedure has been rejected due to the medical risk of the angiography and practical issues that difficult to maintain blindness of investigators. For the primary endpoint, subjects will be followed for 90 days post-randomization. Distribution of the modified Rankin Scale scores at 90 days will be evaluated by two separate assessors who are blinded to treatment. Primary Endpoint will consider central core lab readings only (video interview with RFA method) with local reading as a back-up mechanism.
Allocation
Randomized
Enrollment
376 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
thrombectomy
Arm Type
Experimental
Arm Description
mechanical thrombectomy with stent-retriever and/or thromboaspiration
Arm Title
Clinical treatment
Arm Type
Active Comparator
Arm Description
Best Medical treatment
Intervention Type
Device
Intervention Name(s)
Thrombectomy
Other Intervention Name(s)
Endovascular treatment
Intervention Description
Endovascular treatment of large vessel occlusion (mechanical thrombectomy) with stent-retriever and/or thromboaspiration (neurointerventionalist choice)
Primary Outcome Measure Information:
Title
Modified Rankin Scale scores
Description
Distribution of the modified Rankin Scale scores at 90 days (shift analysis). The score range from zero to 6 with higher values indicating a worst functional outcome at 90 days
Time Frame
90 days
Secondary Outcome Measure Information:
Title
Proportion of Patients with Functional independence in 90 days
Description
Functional independence defined as mRS ≤2
Time Frame
90 days
Title
Disability on the utility-weighted modified Rankin scale (UW-mRS)
Description
Mean score for disability on the utility-weighted modified Rankin scale (UW-mRS). The score range from 1 to zero with higher values indicating a better functional outcome at 90 days
Time Frame
90 days
Title
Quality of life measured by EuroQol Group 5-Dimension Self-Report Questionnaire (EuroQol / EQ5D)
Description
Quality of life analysis as measured by EuroQol/EQ5D 5-Dimension Self-Report Questionnaire, on which scores range from -0.176 to 1, with higher values indicating a better quality of life]) at 90 days
Time Frame
90 days and 1 year
Title
Mortality at 90 days
Description
Mortality at 90 days
Time Frame
90 days
Title
Proportion of patients with Intracranial Hemorrhage at 24 hours
Description
Clinically significant ICH rates at 24 (-2/+12) hours. All intracerebral hemorrhages will be classified by a central core-lab using the Heidelberg criteria. Symptomatic ICH will be defined as per the SITS-MOST definition: deterioration in NIHSS score of ≥4 points within 24 hours from treatment and evidence of intraparenchymal hemorrhage type 2 in the 22 to 36 hours follow-up imaging scans.
Time Frame
24 hours
Title
Procedural related complications
Description
Procedural related complications: arterial perforation, arterial dissection, and embolization in a previously uninvolved vascular territory
Time Frame
immediately after procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Acute ischemic stroke where patient is ineligible for IV thrombolytic treatment or the treatment is contraindicated (e.g., subject presents beyond recommended time from symptom onset), or where patient has received IV thrombolytic therapy without clinical improvement. No significant pre-stroke functional disability (mRS ≤2) Baseline NIHSS score obtained prior to randomization must be equal or higher than 8 points (assessed within one hour prior to qualifying imaging) Age ≥18 years (no upper age limit) Occlusion (TICI 0-1) of the intracranial ICA (distal ICA or T occlusions) and/or MCA-M1 segment suitable for endovascular treatment, as evidenced by CTA, MRA or angiogram, with or without concomitant cervical carotid occlusion or stenosis. The presence of Age-Adjusted modified Clinical ASPECTS Mismatch (mCAM) defined as ASPECTS 5-10 and one of the following criteria: NIHSS ≥ 8 and >50% involvement in 0-1 Cortical (e.g. M1-6) ASPECTS areas (any age); NIHSS ≥ 8 and >50% involvement in 0-2 Cortical (e.g. M1-6) ASPECTS areas (and age < 80 years old); NIHSS ≥ 15 and >50% involvement in 0-3 Cortical (e.g. M1-6) ASPECTS areas (and age < 80 years old). Patient treatable within 6-24 hours of symptom onset. Symptoms onset is defined as point in time the patient was last seen well (at baseline). Treatment start is defined as arterial puncture. Informed consent obtained from patient or acceptable patient surrogate Exclusion Criteria: -Clinical criteria Known hemorrhagic diathesis, coagulation factor deficiency, or oral anticoagulant therapy with INR > 3.0 Baseline platelet count < 30.000/µL Baseline blood glucose of < 50mg/dL Severe, sustained hypertension (SBP > 185 mm Hg or DBP > 110 mm Hg) NOTE: If the blood pressure can be successfully reduced and maintained at the acceptable level using AHA guidelines recommended medication (including iv antihypertensive drips), the patient can be enrolled. Patients in coma defined as totally unresponsive; responding only with reflexes or being areflexic (Intubated patients for transfer could be randomized only in case an NIHSS is obtained by a neurologist prior transportation). Seizures at stroke onset which would preclude obtaining a baseline NIHSS Serious, advanced, or terminal illness with anticipated life expectancy of less than one year. History of life-threatening allergy (more than rash) to contrast medium Subjects who has received IV t-PA treatment beyond 4.5 hours from the beginning of the symptoms Woman of childbearing potential who is known to be pregnant or who has a positive pregnancy test on admission. Subject participating in a study involving an investigational drug or device that would impact this study. Cerebral vasculitis Patients with a pre-existing neurological or psychiatric disease that would confound the neurological or functional evaluations, mRS score at baseline must be ≤2. This excludes patients who are severely demented, require constant assistance in a nursing home type setting or who live at home but are not fully independent in activities of daily living (toileting, dressing, eating, cooking and preparing meals, etc.) Unlikely to be available for 90-day follow-up (e.g. no fixed home address, visitor from overseas). - Neuroimaging criteria Hypodensity on CT or restricted diffusion on MRI amounting to an ASPECTS score of <5. Complete involvement of more than 3 cortical ASPECTS areas (e.g. M1, M2, M3, M4, M5, or M6). Complete absence of leptomeningeal collaterals on CT angiography (e.g. Malignant CTA pattern or score 0). CT or MR evidence of hemorrhage (the presence of GRE microbleeds is allowed). Significant mass effect with midline shift. Evidence of ipsilateral carotid occlusion, high grade stenosis or arterial dissection in the extracranial or petrous segment of the internal carotid artery that cannot be treated or will prevent access to the intracranial clot or excessive tortuosity of cervical vessels precluding device delivery/deployment Subjects with occlusions in multiple vascular territories (e.g., bilateral anterior circulation, or anterior/posterior circulation) Evidence of intracranial tumor (except small meningioma).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sheila CO Martins, MD, PhD
Phone
51999628467
Email
scmartins@hcpa.edu.br
First Name & Middle Initial & Last Name or Official Title & Degree
Natacha Fleck
Phone
51992699829
Email
pesquisaneurovascular@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Raul G Nogueira, MD
Organizational Affiliation
Emory University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sheila CO Martins, MD, PhD
Organizational Affiliation
Hospital de Clinicas de Porto Alegre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Geral de Fortaleza
City
Fortaleza
State/Province
Ceara
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fabricio Lima, PhD
Phone
85999982150
Email
fabricio.lima.neuro@gmail.com
Facility Name
Hospital de Base
City
Brasília
State/Province
DF
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Leticia C Rebello, MD
Phone
61999150626
Email
letirebello@gmail.com
Facility Name
Associacao Congregacao de Santa Catarina
City
Vitória
State/Province
Espirito Santo
ZIP/Postal Code
29050-335
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jose A Fiorot Jr, PhD
Phone
27992778579
Email
fiorotjr@gmail.com
Facility Name
Hospital das Clínicas de Uberlândia
City
Uberlândia
State/Province
Minas Gerais
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jullyanna Shinosaki, MD
Phone
+553491161478
Email
jsm_shinosaki@yahoo.com.br
Facility Name
Hospital de Clínicas da Universidade Federal do Paraná
City
Curitiba
State/Province
Parana
Country
Brazil
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Viviane F Zetola
Phone
0154199761660
Email
viviane.zetola@gmail.com
Facility Name
Conferencia Sao jose do Avai
City
Itaperuna
State/Province
RJ
Country
Brazil
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ivete itaperuna P Goncalves
Phone
22988315201
Email
ipilloster@gmail.com
Facility Name
Hospital de Clinicas de Porto Alegre
City
Porto Alegre
State/Province
RS
ZIP/Postal Code
90035007
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Natacha Fleck
Phone
51992699829
Email
pesquisaneurovascular@gmail.com
First Name & Middle Initial & Last Name & Degree
Ana Julia Lehnen
Phone
51992870762
Email
anajlehnen@gmail.com
Facility Name
Irmandade da Santa Casa de Misericordia de Porto Alegre - ISCMPA
City
Porto Alegre
State/Province
RS
Country
Brazil
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alexandre Maulaz
Phone
51992826915
Email
maulaz@terra.com.br
Facility Name
Hospital das Clínicas da Faculdade de Medicina de Botucatu
City
Botucatu
State/Province
SP
Country
Brazil
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rodrigo Bazan, PhD
Phone
14981157727
Email
bazan.r@terra.com.br
Facility Name
Hospital de Clínicas - UNICAMP
City
Campinas
State/Province
SP
Country
Brazil
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fabricio B Cardoso, MD
Phone
019981254952
Email
fabriciobuchdid@hotmail.com
Facility Name
Hospital das Clinicas de Ribeirao Preto
City
Ribeirão Preto
State/Province
SP
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Octavio M Pontes-Neto, PhD
Phone
16981013465
Email
ompneto@gmail.com
Facility Name
Fundacao Faculdade Regional de Medicina S J Rio Preto
City
São José Do Rio Preto
State/Province
SP
Country
Brazil
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Raquel Hidalgo, MD
Phone
17997640004
Email
draquelhidalgo@gmail.com
Facility Name
Instituto de Assistência Médica ao Servidor Público Estadual de Sao Paulo
City
São Paulo
State/Province
SP
Country
Brazil
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
André Rezende, MD
Phone
+5511981359842
Email
andrerezende@neurointervencao.com.br
Facility Name
Universidade Federal de São Paulo - UNIFESP/EPM
City
São Paulo
State/Province
SP
Country
Brazil
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gisele S Silva, PhD
Email
giselesampaio@hotmail.com

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Because of the sensitive nature of the data collected for this study, requests to access the dataset from qualified researchers trained in human subject confidentiality protocols may be sent to the principal investigators
IPD Sharing Time Frame
after de publication for 6 months
IPD Sharing Access Criteria
Because of the sensitive nature of the data collected for this study, requests to access the dataset from qualified researchers trained in human subject confidentiality protocols may be sent to the principal investigators
Citations:
PubMed Identifier
34850380
Citation
Roaldsen MB, Lindekleiv H, Mathiesen EB. Intravenous thrombolytic treatment and endovascular thrombectomy for ischaemic wake-up stroke. Cochrane Database Syst Rev. 2021 Dec 1;12(12):CD010995. doi: 10.1002/14651858.CD010995.pub3.
Results Reference
derived

Learn more about this trial

Randomization of Endovascular Treatment in Acute Ischemic Stroke in the Extended Time Window

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