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Endovascular Revascularization With Solitaire Device Versus Best Medical Therapy in Anterior Circulation Stroke Within 8 Hours (REVASCAT)

Primary Purpose

Acute Stroke

Status
Terminated
Phase
Phase 3
Locations
Spain
Study Type
Interventional
Intervention
Solitaire FR device
Medical treatment
Sponsored by
Fundacio Ictus Malaltia Vascular
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Stroke focused on measuring Acute ischemic stroke, endovascular treatment, clinical trial

Eligibility Criteria

18 Years - 85 Years (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 recanalization after a minimum of 30 min from start of iv tPA infusion
  • 2. No significant pre-stroke functional disability (mRS ≤ 1)
  • 3. Baseline NIHSS score obtained prior to randomization must be equal or higher than 6 points
  • 4. Age ≥18 and ≤ 85.
  • 5. Occlusion (TICI 0-1) of the intracranial ICA (distal ICA or T occlusions), MCA-M1 segment or tandem proximal ICA/MCA-M1 suitable for endovascular treatment, as evidenced by CTA, MRA or angiogram, with or without concomitant cervical carotid occlusion or stenosis
  • 6. Patient treatable within eight 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 groin puncture.
  • 7. 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 or >400mg/dl
  • 4. Severe, sustained hypertension (SBP > 185 mm Hg or DBP > 110 mm Hg)
  • 5. Patients in coma (NIHSS item of consciousness >1) (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. Renal insufficiency with creatinine ≥ 3 mg/dl
  • 11. Woman of childbearing potential who is known to be pregnant or lactating or who has a positive pregnancy test on admission.
  • 12. Subject participating in a study involving an investigational drug or device that would impact this study.
  • 13. Cerebral vasculitis
  • 14. Patients with a pre-existing neurological or psychiatric disease that would confound the neurological or functional evaluations, mRS score at baseline must be ≤ 1. 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.)
  • 15. Unlikely to be available for 90-day follow-up (e.g. no fixed home address, visitor from overseas).

Neuroimaging criteria:

  • 16. Hypodensity on CT or restricted diffusion amounting to an ASPECTS score of <7 on NCCT or <6 on DWI MRI. Patients 81 to 85 years old with ASPECTS score on non-contrast CT or DWI MRI <9 must be excluded. ASPECTS must be evaluated by CBV maps of CT Perfusion, CTA source imaging (CTA-SI) or DWI-MR in patients whose vascular occlusion study (CTA/MRA) confirming qualifying occlusion, is performed beyond 4.5 hours of last seen well.
  • 17. CT or MR evidence of hemorrhage (the presence of microbleeds is allowed).
  • 18. Significant mass effect with midline shift.
  • 19. 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
  • 20. Subjects with occlusions in multiple vascular territories (e.g., bilateral anterior circulation, or anterior/posterior circulation)
  • 21. Evidence of intracranial tumor (except small meningioma).

Sites / Locations

  • Hospital Germans Trias i Pujol
  • Hospital Universitari Bellvitge
  • Hospital Universitario Vall D'Hebron
  • Hospital Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Endovascular treatment

Medical treatment

Arm Description

Mechanical embolectomy with Solitaire FR device

Medical treatment (standard of care in acute ischemic stroke)including intravenous thrombolysis

Outcomes

Primary Outcome Measures

Between-group comparison of the distribution of the modified Rankin Scale scores (shift analysis)
evaluated by two separate assessors who are blinded to treatment

Secondary Outcome Measures

Mortality at 90 days
Symptomatic Intracerebral Hemorrhage
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 evaluated by independent CT/MR Core Lab and Clinical Events Committee
Infarct Volume
Infarct volume evaluated in a second neuroimaging after treatment evaluated by independent CT/MR Core Lab
Vessel recanalization
Vessel recanalization evaluated by CT angiography or MRA at 24 hours in both treatment groups evaluated by independent CT/MR Core Lab
Intraprocedural related complications in endovascular arm
Procedural related complications in the endovascular treatment arm: arterial perforation, arterial dissection, and embolization in a previously uninvolved vascular territory evaluated by the Angiography Core Lab and the Clinical Events Committee

Full Information

First Posted
September 20, 2012
Last Updated
February 2, 2016
Sponsor
Fundacio Ictus Malaltia Vascular
Collaborators
Medtronic - MITG
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1. Study Identification

Unique Protocol Identification Number
NCT01692379
Brief Title
Endovascular Revascularization With Solitaire Device Versus Best Medical Therapy in Anterior Circulation Stroke Within 8 Hours
Acronym
REVASCAT
Official Title
RandomizEd Trial of reVascularizAtion With Solitaire FR® Device Versus Best mediCal Therapy in the Treatment of Acute Stroke Due to anTerior Circulation Large Vessel Occlusion Presenting Within 8 Hours of Symptom Onset
Study Type
Interventional

2. Study Status

Record Verification Date
February 2016
Overall Recruitment Status
Terminated
Why Stopped
Following DSMB advice after first interim analysis (n=174)
Study Start Date
November 2012 (undefined)
Primary Completion Date
March 2015 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fundacio Ictus Malaltia Vascular
Collaborators
Medtronic - MITG

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To evaluate the hypothesis that mechanical embolectomy with the Solitaire FR device is superior to medical management alone in achieving favorable outcome in the distribution of the modified Rankin Scale scores at 90 days in subjects presenting with acute large vessel ischemic stroke < 8 hours from symptom onset.
Detailed Description
Prospective, multi-center, randomized, controlled, open, blinded-endpoint trial with a sequential design. The randomization employs a 1:1 ratio of mechanical embolectomy with the CE MARK approved stentriever Solitaire FR® versus medical management alone. Randomization will be done under a minimization process using age, baseline NIHSS, therapeutic window and vessel occlusion site. For the primary endpoint, subjects will be followed for 90 days post-randomization. Interim analysis will be performed as preplanned and interpreted by the Data Safety Monitoring Board (DSMB) after the first 174, 346 and 518 patients representing 25%, 50% and 75% of the planned sample size have completed their 90-day follow-up. The DSMB will advise the executive committee (EC) on recommendations to stop the trial early either for reasons of safety, efficacy, futility or to adjust the sample size. The latter may be necessary as given the paucity of data regarding natural history of the non-treated patients assumptions regarding rates of favorable outcomes in this group of patients may be incorrect. Of note, sample size adjustment based on different than expected outcomes rates is permitted, but it is not permitted to adjust the sample size based on change in the pre-specified treatment effect which is set at 10%. Subject population: Subjects presenting with acute ischemic stroke within 8 hours from symptom onset and whose strokes are attributable to an occlusion of the internal carotid or proximal MCA (M1) arteries. Subjects are either ineligible for IV alteplase or have received IV alteplase therapy without recanalization.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Stroke
Keywords
Acute ischemic stroke, endovascular treatment, clinical trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
206 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Endovascular treatment
Arm Type
Experimental
Arm Description
Mechanical embolectomy with Solitaire FR device
Arm Title
Medical treatment
Arm Type
Active Comparator
Arm Description
Medical treatment (standard of care in acute ischemic stroke)including intravenous thrombolysis
Intervention Type
Device
Intervention Name(s)
Solitaire FR device
Intervention Description
Mechanical embolectomy in anterior large vessel occlusion
Intervention Type
Other
Intervention Name(s)
Medical treatment
Intervention Description
Standard of care in acute ischemic stroke including intravenous rTPA
Primary Outcome Measure Information:
Title
Between-group comparison of the distribution of the modified Rankin Scale scores (shift analysis)
Description
evaluated by two separate assessors who are blinded to treatment
Time Frame
90 days after enrollment
Secondary Outcome Measure Information:
Title
Mortality at 90 days
Time Frame
90 days after enrollment
Title
Symptomatic Intracerebral Hemorrhage
Description
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 evaluated by independent CT/MR Core Lab and Clinical Events Committee
Time Frame
24h (-2/+12 hours) after enrollment
Title
Infarct Volume
Description
Infarct volume evaluated in a second neuroimaging after treatment evaluated by independent CT/MR Core Lab
Time Frame
24h (-2/+12h) post treatment
Title
Vessel recanalization
Description
Vessel recanalization evaluated by CT angiography or MRA at 24 hours in both treatment groups evaluated by independent CT/MR Core Lab
Time Frame
24h post treatment
Title
Intraprocedural related complications in endovascular arm
Description
Procedural related complications in the endovascular treatment arm: arterial perforation, arterial dissection, and embolization in a previously uninvolved vascular territory evaluated by the Angiography Core Lab and the Clinical Events Committee
Time Frame
During endovascular treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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 recanalization after a minimum of 30 min from start of iv tPA infusion 2. No significant pre-stroke functional disability (mRS ≤ 1) 3. Baseline NIHSS score obtained prior to randomization must be equal or higher than 6 points 4. Age ≥18 and ≤ 85. 5. Occlusion (TICI 0-1) of the intracranial ICA (distal ICA or T occlusions), MCA-M1 segment or tandem proximal ICA/MCA-M1 suitable for endovascular treatment, as evidenced by CTA, MRA or angiogram, with or without concomitant cervical carotid occlusion or stenosis 6. Patient treatable within eight 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 groin puncture. 7. 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 or >400mg/dl 4. Severe, sustained hypertension (SBP > 185 mm Hg or DBP > 110 mm Hg) 5. Patients in coma (NIHSS item of consciousness >1) (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. Renal insufficiency with creatinine ≥ 3 mg/dl 11. Woman of childbearing potential who is known to be pregnant or lactating or who has a positive pregnancy test on admission. 12. Subject participating in a study involving an investigational drug or device that would impact this study. 13. Cerebral vasculitis 14. Patients with a pre-existing neurological or psychiatric disease that would confound the neurological or functional evaluations, mRS score at baseline must be ≤ 1. 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.) 15. Unlikely to be available for 90-day follow-up (e.g. no fixed home address, visitor from overseas). Neuroimaging criteria: 16. Hypodensity on CT or restricted diffusion amounting to an ASPECTS score of <7 on NCCT or <6 on DWI MRI. Patients 81 to 85 years old with ASPECTS score on non-contrast CT or DWI MRI <9 must be excluded. ASPECTS must be evaluated by CBV maps of CT Perfusion, CTA source imaging (CTA-SI) or DWI-MR in patients whose vascular occlusion study (CTA/MRA) confirming qualifying occlusion, is performed beyond 4.5 hours of last seen well. 17. CT or MR evidence of hemorrhage (the presence of microbleeds is allowed). 18. Significant mass effect with midline shift. 19. 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 20. Subjects with occlusions in multiple vascular territories (e.g., bilateral anterior circulation, or anterior/posterior circulation) 21. Evidence of intracranial tumor (except small meningioma).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Antoni Dávalos, MD
Organizational Affiliation
Hospital Universitario Germans Trias i Pujol, Barcelona, Spain
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Tudor Jovin, MD
Organizational Affiliation
UPMC Stroke Institute, Pittsburgh, PA, USA
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Angel Chamorro, MD
Organizational Affiliation
Hospital Clinic Barcelona, Barcelona, Spain
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Joaquin Serena, MD
Organizational Affiliation
Hospital Josep Trueta, Girona, Spain
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Alex Rovira, MD
Organizational Affiliation
Hospital Vall D'Hebron, Barcelona, Spain
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Maria A De Miquel, MD
Organizational Affiliation
Hospital de Bellvitge, Barcelona, Spain
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Luis Sanromán, MD
Organizational Affiliation
Hospital Clinic, Barcelona, Spain
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Erik Cobo, MD
Organizational Affiliation
UPC, Barcelona, Spain
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Carlos Molina, MD
Organizational Affiliation
Hospital Vall D'Hebron, Barcelona, Spain
Official's Role
Study Director
Facility Information:
Facility Name
Hospital Germans Trias i Pujol
City
Badalona
State/Province
Barcelona
ZIP/Postal Code
08916
Country
Spain
Facility Name
Hospital Universitari Bellvitge
City
Hospitalet de Llobregat
State/Province
Barcelona
ZIP/Postal Code
08907
Country
Spain
Facility Name
Hospital Universitario Vall D'Hebron
City
Barcelona
ZIP/Postal Code
08035
Country
Spain
Facility Name
Hospital Clinic
City
Barcelona
ZIP/Postal Code
08036
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
24206399
Citation
Molina CA, Chamorro A, Rovira A, de Miquel A, Serena J, Roman LS, Jovin TG, Davalos A, Cobo E. REVASCAT: a randomized trial of revascularization with SOLITAIRE FR device vs. best medical therapy in the treatment of acute stroke due to anterior circulation large vessel occlusion presenting within eight-hours of symptom onset. Int J Stroke. 2015 Jun;10(4):619-26. doi: 10.1111/ijs.12157. Epub 2013 Nov 10.
Results Reference
background
PubMed Identifier
30045949
Citation
Kaneko N, Komuro Y, Yokota H, Tateshima S. Stent retrievers with segmented design improve the efficacy of thrombectomy in tortuous vessels. J Neurointerv Surg. 2019 Feb;11(2):119-122. doi: 10.1136/neurintsurg-2018-014061. Epub 2018 Jul 24.
Results Reference
derived
PubMed Identifier
29170266
Citation
Al-Ajlan FS, Al Sultan AS, Minhas P, Assis Z, de Miquel MA, Millan M, San Roman L, Tomassello A, Demchuk AM, Jovin TG, Cuadras P, Davalos A, Goyal M, Menon BK; REVASCAT Investigators. Posttreatment Infarct Volumes when Compared with 24-Hour and 90-Day Clinical Outcomes: Insights from the REVASCAT Randomized Controlled Trial. AJNR Am J Neuroradiol. 2018 Jan;39(1):107-110. doi: 10.3174/ajnr.A5463. Epub 2017 Nov 23.
Results Reference
derived
PubMed Identifier
28318984
Citation
Davalos A, Cobo E, Molina CA, Chamorro A, de Miquel MA, Roman LS, Serena J, Lopez-Cancio E, Ribo M, Millan M, Urra X, Cardona P, Tomasello A, Castano C, Blasco J, Aja L, Rubiera M, Gomis M, Renu A, Lara B, Marti-Fabregas J, Jankowitz B, Cerda N, Jovin TG; REVASCAT Trial Investigators. Safety and efficacy of thrombectomy in acute ischaemic stroke (REVASCAT): 1-year follow-up of a randomised open-label trial. Lancet Neurol. 2017 May;16(5):369-376. doi: 10.1016/S1474-4422(17)30047-9. Epub 2017 Mar 16.
Results Reference
derived
PubMed Identifier
28292867
Citation
Millan M, Remollo S, Quesada H, Renu A, Tomasello A, Minhas P, Perez de la Ossa N, Rubiera M, Llull L, Cardona P, Al-Ajlan F, Hernandez M, Assis Z, Demchuk AM, Jovin T, Davalos A; REVASCAT Trial Investigators. Vessel Patency at 24 Hours and Its Relationship With Clinical Outcomes and Infarct Volume in REVASCAT Trial (Randomized Trial of Revascularization With Solitaire FR Device Versus Best Medical Therapy in the Treatment of Acute Stroke Due to Anterior Circulation Large Vessel Occlusion Presenting Within Eight Hours of Symptom Onset). Stroke. 2017 Apr;48(4):983-989. doi: 10.1161/STROKEAHA.116.015455. Epub 2017 Mar 14.
Results Reference
derived
PubMed Identifier
27940648
Citation
Lopez-Cancio E, Jovin TG, Cobo E, Cerda N, Jimenez M, Gomis M, Hernandez-Perez M, Caceres C, Cardona P, Lara B, Renu A, Llull L, Boned S, Muchada M, Davalos A. Endovascular treatment improves cognition after stroke: A secondary analysis of REVASCAT trial. Neurology. 2017 Jan 17;88(3):245-251. doi: 10.1212/WNL.0000000000003517. Epub 2016 Dec 9.
Results Reference
derived
PubMed Identifier
26956258
Citation
Ribo M, Molina CA, Cobo E, Cerda N, Tomasello A, Quesada H, De Miquel MA, Millan M, Castano C, Urra X, Sanroman L, Davalos A, Jovin T; REVASCAT Trial Investigators. Association Between Time to Reperfusion and Outcome Is Primarily Driven by the Time From Imaging to Reperfusion. Stroke. 2016 Apr;47(4):999-1004. doi: 10.1161/STROKEAHA.115.011721. Epub 2016 Mar 8.
Results Reference
derived
PubMed Identifier
26542697
Citation
Lopez-Cancio E, Salvat M, Cerda N, Jimenez M, Codas J, Llull L, Boned S, Cano LM, Lara B, Molina C, Cobo E, Davalos A, Jovin TG, Serena J; REVASCAT investigators. Phone and Video-Based Modalities of Central Blinded Adjudication of Modified Rankin Scores in an Endovascular Stroke Trial. Stroke. 2015 Dec;46(12):3405-10. doi: 10.1161/STROKEAHA.115.010909. Epub 2015 Nov 5.
Results Reference
derived
PubMed Identifier
26508752
Citation
Urra X, Abilleira S, Dorado L, Ribo M, Cardona P, Millan M, Chamorro A, Molina C, Cobo E, Davalos A, Jovin TG, Gallofre M; Catalan Stroke Code and Reperfusion Consortium. Mechanical Thrombectomy in and Outside the REVASCAT Trial: Insights From a Concurrent Population-Based Stroke Registry. Stroke. 2015 Dec;46(12):3437-42. doi: 10.1161/STROKEAHA.115.011050. Epub 2015 Oct 27.
Results Reference
derived
PubMed Identifier
25882510
Citation
Jovin TG, Chamorro A, Cobo E, de Miquel MA, Molina CA, Rovira A, San Roman L, Serena J, Abilleira S, Ribo M, Millan M, Urra X, Cardona P, Lopez-Cancio E, Tomasello A, Castano C, Blasco J, Aja L, Dorado L, Quesada H, Rubiera M, Hernandez-Perez M, Goyal M, Demchuk AM, von Kummer R, Gallofre M, Davalos A; REVASCAT Trial Investigators. Thrombectomy within 8 hours after symptom onset in ischemic stroke. N Engl J Med. 2015 Jun 11;372(24):2296-306. doi: 10.1056/NEJMoa1503780. Epub 2015 Apr 17.
Results Reference
derived
PubMed Identifier
25428822
Citation
Abilleira S, Ribera A, Davalos A, Ribo M, Chamorro A, Cardona P, Molina CA, Martinez-Yelamos A, Urra X, Dorado L, Roquer J, Marti-Fabregas J, Aja L, Tomasello A, Castano C, Blasco J, Canovas D, Castellanos M, Krupinski J, Guimaraens L, Perendreu J, Ustrell X, Purroy F, Gomez-Choco M, Baiges JJ, Cocho D, Saura J, Gallofre M; Catalan Stroke Code and Reperfusion Consortium. Functional outcome after primary endovascular therapy or IV thrombolysis alone for stroke. An observational, comparative effectiveness study. Cerebrovasc Dis. 2014;38(5):328-36. doi: 10.1159/000368433. Epub 2014 Nov 21.
Results Reference
derived
Links:
URL
http://fundacioictus.com/
Description
Fundacio Ictus is a non-profit organization sponsoring REVASCAT study

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Endovascular Revascularization With Solitaire Device Versus Best Medical Therapy in Anterior Circulation Stroke Within 8 Hours

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