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Efficacy and Safety of MRI-based Thrombolysis in Wake-up Stroke (WAKE-UP)

Primary Purpose

Stroke

Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Alteplase
Placebo
Sponsored by
Universitätsklinikum Hamburg-Eppendorf
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke focused on measuring wake-up stroke, thrombolysis, magnetic resonance imaging (MRI), diffusion weighted imaging (DWI), fluid attenuated inversion recovery (FLAIR)

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Clinical Inclusion Criteria

  • Clinical diagnosis of acute ischemic stroke with unknown symptom onset (e.g., stroke symptoms recognized on awakening)
  • Last known well (without neurological symptoms) > 4.5 hours of treatment initiation
  • Measurable disabling neurological deficit (defined as an impairment of one or more of the following: language, motor function, cognition, gaze, vision, neglect)
  • Age 18-80 years
  • Treatment can be started within 4.5 hours of symptom recognition (e.g., awakening)
  • Written informed consent by patient or proxy

Imaging Inclusion Criteria:

  • Acute stroke MRI including diffusion weighted imaging (DWI) and fluid attenuated inversion recovery (FLAIR) completed
  • MRI showing a pattern of "DWI-FLAIR-mismatch", i.e. acute ischemic lesion visibly on DWI ("positive DWI") but no marked parenchymal hyperintensity visible on FLAIR ("negative FLAIR") indicative of an acute ischemic lesion ≤4.5 hours of age

Exclusion Criteria:

Clinical Exclusion Criteria

  • Planned or anticipated treatment with endovascular reperfusion strategies (e.g. intra-arterial thrombolysis, mechanical recanalization techniques)
  • Pre-stroke disability (inability to carry out all daily activities, requiring some help or supervision, i.e. slight disability corresponding to an MRS score > 1)
  • Participation in any investigational study in the previous 30 days
  • Severe stroke by clinical assessment (e.g. NIHSS > 25)
  • Hypersensitivity to Alteplase or any of the excipients
  • Pregnancy or lactating (formal testing needed in woman of childbearing potential; childbearing potential is assumed in women up to 55 years of age)
  • Significant bleeding disorder at present or within past 6 months
  • Known haemorrhagic diathesis
  • Manifest or recent severe or dangerous bleeding
  • Known history of or suspected intracranial haemorrhage
  • Suspected subarachnoid haemorrhage (even if CT is negative) or condition after subarachnoid haemorrhage from aneurysm
  • History of CNS damage (e.g. neoplasm, aneurysm, intracranial or spinal surgery)
  • Recent (within 10 days) traumatic external heart massage, obstetrical delivery, recent puncture of a non-compressible blood-vessel
  • Current use of anticoagulants (e.g. Phenprocoumon, Warfarin, new anticoagulants such as Dabigatran) or current use of heparin and elevated thromboplastin time (low-dose subcutaneous heparin is allowed)
  • Platelet count < 100.000/mm3 (<100G/l)
  • Blood glucose < 50 or > 400 mg/dl (< 2.8 or 22.2 mmol/l)
  • Severe uncontrolled hypertension, i.e. systolic blood pressure > 185 mmHg or diastolic blood pressure >110 mmHg or requiring aggressive medication to maintain blood pressure within these limits (routine medical treatment is allowed to lower the blood pressure below these limits)
  • Manifest or recent bacterial endocarditis, pericarditis
  • Manifest or recent acute pancreatitis
  • Documented ulcerative gastrointestinal disease during the last 3 months, oesophageal varices, arterial aneurysm, arterial/venous malformations
  • Neoplasm with increased bleeding risk
  • Manifest severe liver disease including hepatic failure, cirrhosis, portal hypertension and active hepatitis
  • Major surgery or significant trauma in past 3 months
  • Stroke within 30 days
  • Life expectancy 6 months or less by judgement of the investigator
  • Any condition associated with a significantly increased risk of severe bleeding not mentioned above
  • Any contraindication to MRI (e.g. cardiac pacemaker)

Imaging Exclusion Criteria:

  • Poor MRI quality precluding interpretation according to the study protocol
  • Any sign of intracranial haemorrhage on baseline MRI
  • FLAIR showing a marked parenchymal hyperintensity in a region corresponding to the acute DWI lesion indicative of an acute ischemic lesion with a high likelihood of being > 4.5 hours old
  • Large DWI lesion volume > 1/3 of the MCA or > 50% of the anterior cerebral artery (ACA) or posterior cerebral artery (PCA) territory (visual inspection) or > 100 ml
  • Any MRI findings indicative of a high risk of symptomatic intracranial haemorrhage related to potential IV-tPA treatment in the judgement of the investigator

Sites / Locations

  • Katholieke Universitet Leuven
  • Aarhus Universitetshospital, Aahrhus Sygehus
  • Hospices Civils de Lyon
  • Charite - Universitätsmedizin Berlin
  • University Medical Center Hamburg-Eppendorf
  • Institut d'Investigacio Biomedica de Girona Doctor Josep Trueta
  • University of Glasgow

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

intravenous tissue plasminogen activator

Placebo

Arm Description

Intervention drug: intravenous tissue plasminogen activator (tPA), alteplase

Intervention drug: placebo

Outcomes

Primary Outcome Measures

Efficacy
Favourable outcome (Modified Rankin Scale 0-1)
Safety
Mortality Death or dependency (Modified Rankin Scale 4-6)

Secondary Outcome Measures

Efficacy
Global outcome score Responder analysis (Modified Rankin Scale 0, 0-1 or 0-2 depending on severity of symptoms assessed by the National Institutes of Health Stroke Scale on admission) Outcome across all disability ranges (categorical shift in Modified Rankin Scale score) Infarct volume (measured 22-36 hours after treatment) Functional health status and quality of life Use of health care system resources
Safety
Symptomatic intracranial haemorrhage (SICH) as defined in SITS-MOST SICH as defined ECASS II SICH as defined in NINDS Parenchymal haemorrhage type 2 (PH-2)

Full Information

First Posted
January 30, 2012
Last Updated
October 9, 2018
Sponsor
Universitätsklinikum Hamburg-Eppendorf
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1. Study Identification

Unique Protocol Identification Number
NCT01525290
Brief Title
Efficacy and Safety of MRI-based Thrombolysis in Wake-up Stroke
Acronym
WAKE-UP
Official Title
Efficacy and Safety of MRI-based Thrombolysis in Wake-up Stroke: a Randomised, Double-blind, Placebo-controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2018
Overall Recruitment Status
Completed
Study Start Date
September 2012 (Actual)
Primary Completion Date
October 2018 (Actual)
Study Completion Date
October 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universitätsklinikum Hamburg-Eppendorf

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
WAKE-UP is an investigator initiated European multicenter randomized controlled clinical trial of MRI based thrombolysis in acute stroke patients with unknown time of symptom onset, e.g. due to recognition of stroke symptoms on awakening. Objective of WAKE-UP is to prove efficacy and safety of MRI-based intravenous thrombolysis with Alteplase in patients waking up with stroke symptoms or patients with otherwise unknown symptom onset.
Detailed Description
WAKE-UP is a clinical trial of MRI based thrombolysis in acute stroke patients with unknown time of symptom onset, e.g. due to recognition of stroke symptoms on awakening. Intravenous thrombolysis with Alteplase is available as effective and safe treatment of acute stroke within 4.5 hours of symptom onset. However, in about 20% of acute stroke patients time of symptom onset is unknown. This large group of patients is currently excluded from treatment with Alteplase. The objective of the research proposed in the WAKE-UP project is to provide effective treatment options for this large group of acute stroke patients. WAKE-UP is designed to prove efficacy and safety of MRI-based intravenous thrombolysis with Alteplase in patients waking up with stroke symptoms or patients with otherwise unknown symptom onset. Patients will be enrolled based on MRI findings indicative of acute ischemic stroke less than 4.5 hours of age.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke
Keywords
wake-up stroke, thrombolysis, magnetic resonance imaging (MRI), diffusion weighted imaging (DWI), fluid attenuated inversion recovery (FLAIR)

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
501 (Actual)

8. Arms, Groups, and Interventions

Arm Title
intravenous tissue plasminogen activator
Arm Type
Experimental
Arm Description
Intervention drug: intravenous tissue plasminogen activator (tPA), alteplase
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Intervention drug: placebo
Intervention Type
Drug
Intervention Name(s)
Alteplase
Other Intervention Name(s)
Actilyse, Activase, rt-PA
Intervention Description
Intravenous tissue plasminogen activator (Alteplase) 0.9 mg/kg body-weight up to a maximum of 90 mg, 10% as bolus, 90% over 1 hour as infusion
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
lyophilised powder to be reconstituted as solution indistinguishable from the active drug
Primary Outcome Measure Information:
Title
Efficacy
Description
Favourable outcome (Modified Rankin Scale 0-1)
Time Frame
90 day after stroke
Title
Safety
Description
Mortality Death or dependency (Modified Rankin Scale 4-6)
Time Frame
90 day after stroke
Secondary Outcome Measure Information:
Title
Efficacy
Description
Global outcome score Responder analysis (Modified Rankin Scale 0, 0-1 or 0-2 depending on severity of symptoms assessed by the National Institutes of Health Stroke Scale on admission) Outcome across all disability ranges (categorical shift in Modified Rankin Scale score) Infarct volume (measured 22-36 hours after treatment) Functional health status and quality of life Use of health care system resources
Time Frame
90 days after stroke
Title
Safety
Description
Symptomatic intracranial haemorrhage (SICH) as defined in SITS-MOST SICH as defined ECASS II SICH as defined in NINDS Parenchymal haemorrhage type 2 (PH-2)
Time Frame
90 days after stroke

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinical Inclusion Criteria Clinical diagnosis of acute ischemic stroke with unknown symptom onset (e.g., stroke symptoms recognized on awakening) Last known well (without neurological symptoms) > 4.5 hours of treatment initiation Measurable disabling neurological deficit (defined as an impairment of one or more of the following: language, motor function, cognition, gaze, vision, neglect) Age 18-80 years Treatment can be started within 4.5 hours of symptom recognition (e.g., awakening) Written informed consent by patient or proxy Imaging Inclusion Criteria: Acute stroke MRI including diffusion weighted imaging (DWI) and fluid attenuated inversion recovery (FLAIR) completed MRI showing a pattern of "DWI-FLAIR-mismatch", i.e. acute ischemic lesion visibly on DWI ("positive DWI") but no marked parenchymal hyperintensity visible on FLAIR ("negative FLAIR") indicative of an acute ischemic lesion ≤4.5 hours of age Exclusion Criteria: Clinical Exclusion Criteria Planned or anticipated treatment with endovascular reperfusion strategies (e.g. intra-arterial thrombolysis, mechanical recanalization techniques) Pre-stroke disability (inability to carry out all daily activities, requiring some help or supervision, i.e. slight disability corresponding to an MRS score > 1) Participation in any investigational study in the previous 30 days Severe stroke by clinical assessment (e.g. NIHSS > 25) Hypersensitivity to Alteplase or any of the excipients Pregnancy or lactating (formal testing needed in woman of childbearing potential; childbearing potential is assumed in women up to 55 years of age) Significant bleeding disorder at present or within past 6 months Known haemorrhagic diathesis Manifest or recent severe or dangerous bleeding Known history of or suspected intracranial haemorrhage Suspected subarachnoid haemorrhage (even if CT is negative) or condition after subarachnoid haemorrhage from aneurysm History of CNS damage (e.g. neoplasm, aneurysm, intracranial or spinal surgery) Recent (within 10 days) traumatic external heart massage, obstetrical delivery, recent puncture of a non-compressible blood-vessel Current use of anticoagulants (e.g. Phenprocoumon, Warfarin, new anticoagulants such as Dabigatran) or current use of heparin and elevated thromboplastin time (low-dose subcutaneous heparin is allowed) Platelet count < 100.000/mm3 (<100G/l) Blood glucose < 50 or > 400 mg/dl (< 2.8 or 22.2 mmol/l) Severe uncontrolled hypertension, i.e. systolic blood pressure > 185 mmHg or diastolic blood pressure >110 mmHg or requiring aggressive medication to maintain blood pressure within these limits (routine medical treatment is allowed to lower the blood pressure below these limits) Manifest or recent bacterial endocarditis, pericarditis Manifest or recent acute pancreatitis Documented ulcerative gastrointestinal disease during the last 3 months, oesophageal varices, arterial aneurysm, arterial/venous malformations Neoplasm with increased bleeding risk Manifest severe liver disease including hepatic failure, cirrhosis, portal hypertension and active hepatitis Major surgery or significant trauma in past 3 months Stroke within 30 days Life expectancy 6 months or less by judgement of the investigator Any condition associated with a significantly increased risk of severe bleeding not mentioned above Any contraindication to MRI (e.g. cardiac pacemaker) Imaging Exclusion Criteria: Poor MRI quality precluding interpretation according to the study protocol Any sign of intracranial haemorrhage on baseline MRI FLAIR showing a marked parenchymal hyperintensity in a region corresponding to the acute DWI lesion indicative of an acute ischemic lesion with a high likelihood of being > 4.5 hours old Large DWI lesion volume > 1/3 of the MCA or > 50% of the anterior cerebral artery (ACA) or posterior cerebral artery (PCA) territory (visual inspection) or > 100 ml Any MRI findings indicative of a high risk of symptomatic intracranial haemorrhage related to potential IV-tPA treatment in the judgement of the investigator
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christian Gerloff, MD
Organizational Affiliation
Universitätsklinikum Hamburg-Eppendorf
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Goetz Thomalla, MD
Organizational Affiliation
Universitätsklinikum Hamburg-Eppendorf
Official's Role
Principal Investigator
Facility Information:
Facility Name
Katholieke Universitet Leuven
City
Leuven
ZIP/Postal Code
3000
Country
Belgium
Facility Name
Aarhus Universitetshospital, Aahrhus Sygehus
City
Aarhus
ZIP/Postal Code
8000
Country
Denmark
Facility Name
Hospices Civils de Lyon
City
Bron Cedex
ZIP/Postal Code
69677
Country
France
Facility Name
Charite - Universitätsmedizin Berlin
City
Berlin
ZIP/Postal Code
10117
Country
Germany
Facility Name
University Medical Center Hamburg-Eppendorf
City
Hamburg
ZIP/Postal Code
20246
Country
Germany
Facility Name
Institut d'Investigacio Biomedica de Girona Doctor Josep Trueta
City
Girona
ZIP/Postal Code
17007
Country
Spain
Facility Name
University of Glasgow
City
Glasgow
ZIP/Postal Code
G12 8QQ
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
29766770
Citation
Thomalla G, Simonsen CZ, Boutitie F, Andersen G, Berthezene Y, Cheng B, Cheripelli B, Cho TH, Fazekas F, Fiehler J, Ford I, Galinovic I, Gellissen S, Golsari A, Gregori J, Gunther M, Guibernau J, Hausler KG, Hennerici M, Kemmling A, Marstrand J, Modrau B, Neeb L, Perez de la Ossa N, Puig J, Ringleb P, Roy P, Scheel E, Schonewille W, Serena J, Sunaert S, Villringer K, Wouters A, Thijs V, Ebinger M, Endres M, Fiebach JB, Lemmens R, Muir KW, Nighoghossian N, Pedraza S, Gerloff C; WAKE-UP Investigators. MRI-Guided Thrombolysis for Stroke with Unknown Time of Onset. N Engl J Med. 2018 Aug 16;379(7):611-622. doi: 10.1056/NEJMoa1804355. Epub 2018 May 16.
Results Reference
result
PubMed Identifier
35769368
Citation
Barow E, Quandt F, Cheng B, Gelderblom M, Jensen M, Konigsberg A, Boutitie F, Nighoghossian N, Ebinger M, Endres M, Fiebach JB, Thijs V, Lemmens R, Muir KW, Pedraza S, Simonsen CZ, Gerloff C, Thomalla G. Association of White Blood Cell Count With Clinical Outcome Independent of Treatment With Alteplase in Acute Ischemic Stroke. Front Neurol. 2022 Jun 13;13:877367. doi: 10.3389/fneur.2022.877367. eCollection 2022.
Results Reference
derived
PubMed Identifier
34782419
Citation
Schlemm L, Braemswig TB, Boutitie F, Vynckier J, Jensen M, Galinovic I, Simonsen CZ, Cheng B, Cho TH, Fiehler J, Puig J, Thijs V, Fiebach J, Muir K, Nighoghossian N, Ebinger M, Pedraza S, Thomalla G, Gerloff C, Endres M, Lemmens R, Nolte CH; WAKE-UP Investigators. Cerebral Microbleeds and Treatment Effect of Intravenous Thrombolysis in Acute Stroke: An Analysis of the WAKE-UP Randomized Clinical Trial. Neurology. 2022 Jan 18;98(3):e302-e314. doi: 10.1212/WNL.0000000000013055. Epub 2021 Nov 15.
Results Reference
derived
PubMed Identifier
34433305
Citation
Lettow I, Jensen M, Schlemm E, Boutitie F, Quandt F, Cheng B, Ebinger M, Endres M, Fiebach JB, Thijs V, Lemmens R, Muir KW, Nighoghossian N, Pedraza S, Simonsen CZ, Gerloff C, Thomalla G; WAKE-UP Investigators. Serious Adverse Events and Their Impact on Functional Outcome in Acute Ischemic Stroke in the WAKE-UP Trial. Stroke. 2021 Dec;52(12):3768-3776. doi: 10.1161/STROKEAHA.120.033425. Epub 2021 Aug 26.
Results Reference
derived
PubMed Identifier
34414292
Citation
Barow E, Boutitie F, Cheng B, Cho TH, Ebinger M, Endres M, Fiebach JB, Fiehler J, Nickel A, Puig J, Roy P, Lemmens R, Thijs V, Muir KW, Nighoghossian N, Pedraza S, Simonsen CZ, Gerloff C, Thomalla G. 24-hour blood pressure variability and treatment effect of intravenous alteplase in acute ischaemic stroke. Eur Stroke J. 2021 Jun;6(2):168-175. doi: 10.1177/23969873211014758. Epub 2021 Jun 18.
Results Reference
derived
PubMed Identifier
33980046
Citation
Scheldeman L, Wouters A, Dupont P, Christensen S, Boutitie F, Cheng B, Ebinger M, Endres M, Fiebach JB, Gerloff C, Muir KW, Nighoghossian N, Pedraza S, Simonsen CZ, Ringelstein EB, Chamorro A, Grond M, Laage R, Schneider A, Thomalla G, Thijs V, Lemmens R. Reversible Edema in the Penumbra Correlates With Severity of Hypoperfusion. Stroke. 2021 Jul;52(7):2338-2346. doi: 10.1161/STROKEAHA.120.033071. Epub 2021 May 13.
Results Reference
derived
PubMed Identifier
33657675
Citation
Konigsberg A, Sehner S, Arlt S, Cheng B, Simonsen CZ, Boutitie F, Serena J, Thijs V, Ebinger M, Endres M, Fiebach JB, Lemmens R, Muir KW, Nighoghossian N, Pedraza S, Gerloff C, Thomalla G; WAKE-UP investigators. Effect of intravenous alteplase on post-stroke depression in the WAKE UP trial. Eur J Neurol. 2021 Jun;28(6):2017-2025. doi: 10.1111/ene.14797. Epub 2021 Mar 22.
Results Reference
derived
PubMed Identifier
33613422
Citation
Grosch AS, Kufner A, Boutitie F, Cheng B, Ebinger M, Endres M, Fiebach JB, Fiehler J, Konigsberg A, Lemmens R, Muir KW, Nighoghossian N, Pedraza S, Siemonsen CZ, Thijs V, Wouters A, Gerloff C, Thomalla G, Galinovic I. Extent of FLAIR Hyperintense Vessels May Modify Treatment Effect of Thrombolysis: A Post hoc Analysis of the WAKE-UP Trial. Front Neurol. 2021 Feb 4;11:623881. doi: 10.3389/fneur.2020.623881. eCollection 2020.
Results Reference
derived
PubMed Identifier
33324925
Citation
Barow E, Pinnschmidt H, Boutitie F, Konigsberg A, Ebinger M, Endres M, Fiebach JB, Fiehler J, Thijs V, Lemmens R, Muir KW, Nighoghossian N, Pedraza S, Simonsen CZ, Gerloff C, Thomalla G, Cheng B; WAKE-UP investigators. Symptoms and probabilistic anatomical mapping of lacunar infarcts. Neurol Res Pract. 2020 Aug 3;2:21. doi: 10.1186/s42466-020-00068-y. eCollection 2020.
Results Reference
derived
PubMed Identifier
31824412
Citation
Schlemm L, Kufner A, Boutitie F, Nave AH, Gerloff C, Thomalla G, Simonsen CZ, Ford I, Lemmens R, Muir KW, Nighoghossian N, Pedraza S, Ebinger M, Endres M. Current Smoking Does Not Modify the Treatment Effect of Intravenous Thrombolysis in Acute Ischemic Stroke Patients-A Post-hoc Analysis of the WAKE-UP Trial. Front Neurol. 2019 Nov 22;10:1239. doi: 10.3389/fneur.2019.01239. eCollection 2019.
Results Reference
derived
PubMed Identifier
31161343
Citation
Barow E, Boutitie F, Cheng B, Cho TH, Ebinger M, Endres M, Fiebach JB, Fiehler J, Ford I, Galinovic I, Nickel A, Puig J, Roy P, Wouters A, Thijs V, Lemmens R, Muir KW, Nighoghossian N, Pedraza S, Simonsen CZ, Gerloff C, Thomalla G; WAKE-UP investigators. Clinical Characteristics and Outcome of Patients with Lacunar Infarcts and Concurrent Embolic Ischemic Lesions. Clin Neuroradiol. 2020 Sep;30(3):511-516. doi: 10.1007/s00062-019-00800-5. Epub 2019 Jun 3.
Results Reference
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PubMed Identifier
28842449
Citation
Thomalla G, Boutitie F, Fiebach JB, Simonsen CZ, Nighoghossian N, Pedraza S, Lemmens R, Roy P, Muir KW, Heesen C, Ebinger M, Ford I, Cheng B, Cho TH, Puig J, Thijs V, Endres M, Fiehler J, Gerloff C. Effect of informed consent on patient characteristics in a stroke thrombolysis trial. Neurology. 2017 Sep 26;89(13):1400-1407. doi: 10.1212/WNL.0000000000004414. Epub 2017 Aug 25.
Results Reference
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PubMed Identifier
28425349
Citation
Thomalla G, Boutitie F, Fiebach JB, Simonsen CZ, Pedraza S, Lemmens R, Nighoghossian N, Roy P, Muir KW, Ebinger M, Ford I, Cheng B, Galinovic I, Cho TH, Puig J, Thijs V, Endres M, Fiehler J, Gerloff C. Clinical characteristics of unknown symptom onset stroke patients with and without diffusion-weighted imaging and fluid-attenuated inversion recovery mismatch. Int J Stroke. 2018 Jan;13(1):66-73. doi: 10.1177/1747493017706245. Epub 2017 Apr 20.
Results Reference
derived
PubMed Identifier
28174327
Citation
Thomalla G, Boutitie F, Fiebach JB, Simonsen CZ, Nighoghossian N, Pedraza S, Lemmens R, Roy P, Muir KW, Ebinger M, Ford I, Cheng B, Galinovic I, Cho TH, Puig J, Thijs V, Endres M, Fiehler J, Gerloff C; WAKE-UP Investigators. Stroke With Unknown Time of Symptom Onset: Baseline Clinical and Magnetic Resonance Imaging Data of the First Thousand Patients in WAKE-UP (Efficacy and Safety of MRI-Based Thrombolysis in Wake-Up Stroke: A Randomized, Doubleblind, Placebo-Controlled Trial). Stroke. 2017 Mar;48(3):770-773. doi: 10.1161/STROKEAHA.116.015233. Epub 2017 Feb 7.
Results Reference
derived

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Efficacy and Safety of MRI-based Thrombolysis in Wake-up Stroke

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