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Thrombectomy REvascularization of Large Vessel Occlusions in Acute Ischemic Stroke (TREVO) (TREVO)

Primary Purpose

Ischemic Stroke

Status
Completed
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
Mechanical Thrombectomy
Sponsored by
Stryker Neurovascular
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ischemic Stroke focused on measuring Stroke, Ischemic, Thrombus, Embolectomy, Thrombectomy, Concentric, Embolus, Mechanical, Trevo

Eligibility Criteria

18 Years - 79 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18-79 (has had 18th birthday, but not yet had 80th birthday)
  • NIHSS 8 - 30
  • Anticipated life expectancy of at least 6 months
  • No significant pre-stroke disability (mRS less than or equal to 1)
  • Written informed consent to participate given by patient or legal representative
  • Angiographic confirmation of a persistent large vessel occlusion, in the internal carotid, middle cerebral M1 and/or M2 segments, basilar or vertebral arteries
  • Treatable within 8 hours of symptom onset, defined as the first pass being made with the Trevo device.

Exclusion Criteria:

  • Baseline glucose of < 50 mg/dL (2.78 mmol) or > 400 mg / dL (22.20 mmol)
  • Known hemorrhagic diathesis, coagulation factor deficiency, or oral anticoagulant therapy with INR > 3.0
  • Treated with Heparin within 48 hours with a PTT greater than 2 times the lab normal
  • Baseline platelet count < 30,000
  • History of severe allergy (more than rash) to contrast medium
  • 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 medication (i.e. Nipride), the patient can be enrolled
  • Woman of child bearing potential who is known to be pregnant
  • Patient participating in another clinical study or protocol
  • For anterior circulation strokes: strokes involving greater than 1/3 of the MCA territory, as determined by hypodensity on the baseline non- contrast CT, or low CBV on CT Perfusion imaging, or restricted diffusion on DWI images
  • For posterior circulation strokes within the midbrain and/or pons, extensive hypodensity on the baseline CT, or low CBV on CT Perfusion imaging, or extensive restricted diffusion on DWI images
  • Baseline CT/MR evidence of significant mass effect with midline shift
  • Baseline CT/MR evidence of hemorrhage
  • Baseline CT/MR evidence of intracranial tumor (except small meningioma)
  • Angiographic evidence of vasculitis or arterial dissection
  • High grade stenosis that cannot be treated safely or which prevents access to the thrombus with the Trevo device
  • Angiographic evidence of excessive arterial tortuosity that precludes the Trevo device from reaching the thrombus

Sites / Locations

  • Christian Doppler Clinic
  • Universitätsklinik Göttingen
  • University Hospital Schleswig-Holstein Campus Kiel
  • Technische Universität München
  • Hospital Clínic de Barcelona
  • Hospital Universitari Germans Trias i Pujols
  • Karolinska University Hospital

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Acute Ischemic Stroke

Arm Description

Single arm post market surveillance study for CE marked mechanical thrombectomy device, Trevo retriever for treatment of eligible patients experiencing acute ischemic stroke Mechanical thrombectomy intervention for all subjects in Acute Ischemic Stroke

Outcomes

Primary Outcome Measures

Revascularization Status
Revascularization, defined as at least TICI 2a in the vascular territory treated at end of the neuro interventional procedure Thrombolysis in Cerebral Infarction (TICI) grading system for perfusion (ie blood flow through a vessel) Grade 0:No Perfusion. No antegrade flow beyond the point of occlusion. Grade 1:Penetration With Minimal Perfusion. Grade 2:Partial Perfusion. Grade 2a:Only partial filling (<2/3) of the entire vascular territory is visualized. Grade 2b:Complete filling of all of the expected vascular territory is visualized, but slower ... Grade 3:Complete Perfusion. For complete info see Higashida RT, Furlan AJ, Roberts H, Tomsick T, Connors B et al. (2003) Trial design and reporting standards for intra-arterial cerebral thrombolysis for acute ischemic stroke. Stroke 34: e109-e137.10.1161/01.STR.0000082721.62796.09 PubMed: 12869717[PubMed]

Secondary Outcome Measures

Clinical Outcomes at 90 Days
Good clinical outcome is defined as an modified Rankin Scale (mRS) score of 0-2 at 90 days. mRS 0-2 indicates functional independence 0 - No symptoms. - No significant disability. Able to carry out all usual activities, despite some symptoms. - Slight disability. Able to look after own affairs without assistance, but unable to carry out all previous activities. - Moderate disability. Requires some help, but able to walk unassisted. - Moderately severe disability. Unable to attend to own bodily needs without assistance, and unable to walk unassisted. - Severe disability. Requires constant nursing care and attention, bedridden, incontinent. - Dead. https://en.wikipedia.org/wiki/Modified_Rankin_Scale
Mortality at 90 Days
All cause mortality through 90 days post procedure.

Full Information

First Posted
March 15, 2010
Last Updated
July 13, 2015
Sponsor
Stryker Neurovascular
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1. Study Identification

Unique Protocol Identification Number
NCT01088672
Brief Title
Thrombectomy REvascularization of Large Vessel Occlusions in Acute Ischemic Stroke (TREVO)
Acronym
TREVO
Official Title
Thrombectomy REvascularization of Large Vessel Occlusions in Acute Ischemic Stroke (TREVO)
Study Type
Interventional

2. Study Status

Record Verification Date
July 2015
Overall Recruitment Status
Completed
Study Start Date
February 2010 (undefined)
Primary Completion Date
August 2011 (Actual)
Study Completion Date
November 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Stryker Neurovascular

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
To determine the revascularization rate of the CE-marked Trevo device in large vessel occlusions in ischemic stroke patients. Revascularization, defined as at least TICI 2a in the vascular territory treated at end of the neuro interventional procedure.
Detailed Description
Clinical outcomes at 90 days Mortality at 90 days Device-related serious adverse events (DRSAEs) Symptomatic ICH rate within 24 (-6/+12) hours post-procedure

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ischemic Stroke
Keywords
Stroke, Ischemic, Thrombus, Embolectomy, Thrombectomy, Concentric, Embolus, Mechanical, Trevo

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Acute Ischemic Stroke
Arm Type
Other
Arm Description
Single arm post market surveillance study for CE marked mechanical thrombectomy device, Trevo retriever for treatment of eligible patients experiencing acute ischemic stroke Mechanical thrombectomy intervention for all subjects in Acute Ischemic Stroke
Intervention Type
Procedure
Intervention Name(s)
Mechanical Thrombectomy
Other Intervention Name(s)
Trevo Procedure
Intervention Description
The Trevo device is intended to restore blood flow in the neurovasculature by removing thrombus in patients experiencing ischemic stroke.
Primary Outcome Measure Information:
Title
Revascularization Status
Description
Revascularization, defined as at least TICI 2a in the vascular territory treated at end of the neuro interventional procedure Thrombolysis in Cerebral Infarction (TICI) grading system for perfusion (ie blood flow through a vessel) Grade 0:No Perfusion. No antegrade flow beyond the point of occlusion. Grade 1:Penetration With Minimal Perfusion. Grade 2:Partial Perfusion. Grade 2a:Only partial filling (<2/3) of the entire vascular territory is visualized. Grade 2b:Complete filling of all of the expected vascular territory is visualized, but slower ... Grade 3:Complete Perfusion. For complete info see Higashida RT, Furlan AJ, Roberts H, Tomsick T, Connors B et al. (2003) Trial design and reporting standards for intra-arterial cerebral thrombolysis for acute ischemic stroke. Stroke 34: e109-e137.10.1161/01.STR.0000082721.62796.09 PubMed: 12869717[PubMed]
Time Frame
Post-procedure, immediate=at the end of the procedure, per last angiogram during treatment
Secondary Outcome Measure Information:
Title
Clinical Outcomes at 90 Days
Description
Good clinical outcome is defined as an modified Rankin Scale (mRS) score of 0-2 at 90 days. mRS 0-2 indicates functional independence 0 - No symptoms. - No significant disability. Able to carry out all usual activities, despite some symptoms. - Slight disability. Able to look after own affairs without assistance, but unable to carry out all previous activities. - Moderate disability. Requires some help, but able to walk unassisted. - Moderately severe disability. Unable to attend to own bodily needs without assistance, and unable to walk unassisted. - Severe disability. Requires constant nursing care and attention, bedridden, incontinent. - Dead. https://en.wikipedia.org/wiki/Modified_Rankin_Scale
Time Frame
90-day
Title
Mortality at 90 Days
Description
All cause mortality through 90 days post procedure.
Time Frame
90-day

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
79 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18-79 (has had 18th birthday, but not yet had 80th birthday) NIHSS 8 - 30 Anticipated life expectancy of at least 6 months No significant pre-stroke disability (mRS less than or equal to 1) Written informed consent to participate given by patient or legal representative Angiographic confirmation of a persistent large vessel occlusion, in the internal carotid, middle cerebral M1 and/or M2 segments, basilar or vertebral arteries Treatable within 8 hours of symptom onset, defined as the first pass being made with the Trevo device. Exclusion Criteria: Baseline glucose of < 50 mg/dL (2.78 mmol) or > 400 mg / dL (22.20 mmol) Known hemorrhagic diathesis, coagulation factor deficiency, or oral anticoagulant therapy with INR > 3.0 Treated with Heparin within 48 hours with a PTT greater than 2 times the lab normal Baseline platelet count < 30,000 History of severe allergy (more than rash) to contrast medium 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 medication (i.e. Nipride), the patient can be enrolled Woman of child bearing potential who is known to be pregnant Patient participating in another clinical study or protocol For anterior circulation strokes: strokes involving greater than 1/3 of the MCA territory, as determined by hypodensity on the baseline non- contrast CT, or low CBV on CT Perfusion imaging, or restricted diffusion on DWI images For posterior circulation strokes within the midbrain and/or pons, extensive hypodensity on the baseline CT, or low CBV on CT Perfusion imaging, or extensive restricted diffusion on DWI images Baseline CT/MR evidence of significant mass effect with midline shift Baseline CT/MR evidence of hemorrhage Baseline CT/MR evidence of intracranial tumor (except small meningioma) Angiographic evidence of vasculitis or arterial dissection High grade stenosis that cannot be treated safely or which prevents access to the thrombus with the Trevo device Angiographic evidence of excessive arterial tortuosity that precludes the Trevo device from reaching the thrombus
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nils Wahlgren, MD
Organizational Affiliation
Karolinska University Hospital in Solna
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Olav Jansen, MD
Organizational Affiliation
Universitätsklinikum Schleswig-Holstein - Campus Kiel UK S-H
Official's Role
Principal Investigator
Facility Information:
Facility Name
Christian Doppler Clinic
City
Salzburg
Country
Austria
Facility Name
Universitätsklinik Göttingen
City
Gottingen
Country
Germany
Facility Name
University Hospital Schleswig-Holstein Campus Kiel
City
Kiel
Country
Germany
Facility Name
Technische Universität München
City
Munich
Country
Germany
Facility Name
Hospital Clínic de Barcelona
City
Barcelona
ZIP/Postal Code
08036
Country
Spain
Facility Name
Hospital Universitari Germans Trias i Pujols
City
Barcelona
Country
Spain
Facility Name
Karolinska University Hospital
City
Stockholm
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
24135533
Citation
Jansen O, Macho JM, Killer-Oberpfalzer M, Liebeskind D, Wahlgren N; TREVO Study Group. Neurothrombectomy for the treatment of acute ischemic stroke: results from the TREVO study. Cerebrovasc Dis. 2013;36(3):218-25. doi: 10.1159/000353990. Epub 2013 Oct 12.
Results Reference
result
PubMed Identifier
24876082
Citation
Shi ZS, Liebeskind DS, Xiang B, Ge SG, Feng L, Albers GW, Budzik R, Devlin T, Gupta R, Jansen O, Jovin TG, Killer-Oberpfalzer M, Lutsep HL, Macho J, Nogueira RG, Rymer M, Smith WS, Wahlgren N, Duckwiler GR; Multi MERCI, TREVO, and TREVO 2 Investigators. Predictors of functional dependence despite successful revascularization in large-vessel occlusion strokes. Stroke. 2014 Jul;45(7):1977-84. doi: 10.1161/STROKEAHA.114.005603. Epub 2014 May 29.
Results Reference
derived

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Thrombectomy REvascularization of Large Vessel Occlusions in Acute Ischemic Stroke (TREVO)

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