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Treatment With Intent to Generate Endovascular Reperfusion (TIGER)

Primary Purpose

Ischemic Stroke

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Tigertriever revascularization device
Sponsored by
Rapid Medical
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ischemic Stroke focused on measuring Mechanical thrombectomy,, Brain, Brain clot, Brain infarction, Cerebral ischemia, Neurovascular intervention, Revascularization, Reperfusion, Stent retriever, Tigertriever, Stroke, Rapid Medical

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. New focal neurologic deficit consistent with being of acute cerebral ischemia origin.
  2. Age 18-85 years old (inclusive).
  3. Interventionalist estimates that treatment with the Tigertriever (first deployment in target vessel) can be achieved within 8 hours of symptom onset.
  4. Patient either: a) eligible for, and received, IV t-PA within 3 hours of symptom onset, at the correct 0.9 mg/kg dose, or b) ineligible for IV t-PA.
  5. NIH Stroke Scale score of 8-29.
  6. No known significant pre-stroke disability (prestroke mRS 0 or 1).
  7. Catheter angiographic confirmation of a large vessel occlusion in the intracranial internal carotid artery, the M1 or M2 segments of the middle cerebral artery, the intracranial vertebral artery, or the basilar artery that is accessible to Tigertriever device.
  8. For strokes in the anterior circulation, the following imaging criteria should also be met:

    1. MRI criterion: volume of diffusion restriction visually assessed ≤50 mL, OR
    2. CT criterion: ASPECTS 6 to 10 on baseline NCCT or CTA-source images,
  9. For strokes in the posterior circulation, the following imaging criterion should also be met: pcASPECTS score 8 to 10 on baseline NCCT, CTA-source images, or DWI MRI.
  10. Anticipated life expectancy of at least 6 months.
  11. A signed informed consent by patient or a Legally Authorized Representative or independent physician in case of oral consent.

Exclusion Criteria:

  1. Subject already participating in another study of an investigational treatment device or treatment.
  2. Use of any other intra-arterial recanalization drug or device prior to the Tigertriever (Tigertriever not as first choice device).
  3. Angiographically evident excessive arterial tortuosity precluding device access to the thrombus.
  4. For all patients, severe sustained hypertension with SBP >220 and/or DBP >120; for patients treated with IV tPA, sustained hypertension despite treatment with SBP >185 and/or DBP > 110.
  5. Glucose < 50 mg/dl (2.78 mmol/L) or > 400 mg/dl (22.20 mmol/L).
  6. Known hemorrhagic diathesis.
  7. Coagulation factor deficiency or oral anti-coagulant therapy with an international normalized ratio (INR) of more than 3.0.
  8. Treatment with heparin within 48 h with a partial thromboplastin time more than two times the laboratory normal.
  9. Patients who have received a direct thrombin inhibitor within the last 48 hours; must have a partial thromboplastin time (PTT) less than 1.5 times the normal to be eligible.
  10. Platelet count of less than 50,000/uL.
  11. History of severe allergy to contrast medium, nickel, or Nitinol.
  12. Intracranial hemorrhage.
  13. Significant mass effect with midline shift.
  14. Intracranial tumor (apart from small meningioma, ≤ 2 cm in diameter).
  15. Stenosis or any occlusion in the deployment site or in a proximal vessel requiring treatment or preventing device access to the thrombus (for example, stenosis or occlusion in the cervical internal carotid artery).
  16. Females who are pregnant or breastfeeding.
  17. Known current use of cocaine at time of treatment.
  18. Prior recent stroke in the past 3 months.
  19. Renal failure with serum creatinine >3.0 or Glomerular Filtration Rate (GFR) <30.
  20. Known cerebral vasculitis.
  21. Rapidly improving neurological status defined as improvement of greater than 8 points on the NIHSS or improvement to NIHSS of < 6 prior to procedure
  22. Clinical symptoms suggestive of bilateral stroke or stroke in multiple territories.
  23. Ongoing seizure due to stroke.
  24. Evidence of active systemic infection.
  25. Known cancer with metastases.
  26. Suspicion of aortic dissection, septic embolus, or bacterial endocarditis.
  27. Evidence of dissection in the extra or intracranial cerebral arteries.
  28. Occlusions in multiple vascular territories (e.g., bilateral anterior circulation, or anterior/posterior circulation).
  29. Aneurysm in target vessel.

Sites / Locations

  • UCLA medical center
  • Los Robles
  • Tenet Health
  • Baptist Health Research Institute
  • Baptist Health South Florida
  • University of Miami
  • WellStar Research Institute
  • University of Iowa
  • University of Massachusetts
  • Maimonides Medical Center
  • University of Buffalo
  • Riverside Methodist Hospital
  • Mercy Health
  • Oregon Health & Science University
  • UPMC
  • VBMC Harlingen
  • Rambam

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Tigertriever revascularization device

Arm Description

Mechanical thrombectomy with Tigertriever

Outcomes

Primary Outcome Measures

Successful reperfusion, defined as mTICI Score ≥ 2b
Effectiveness (Successful reperfusion)
All-cause mortality
Safety (All-cause mortality)
Symptomatic intracranial hemorrhage (sICH) defined as any parenchymal hematoma type 2, remote intracerebral hemorrhage, subarachnoid hemorrhage, or intraventricular hemorrhage that is the predominant cause of ≥4 point NIHSS deterioration at 24 hours
Safety (Symptomatic intracranial hemorrhage (sICH)) defined as any parenchymal hematoma type 2, remote intracerebral hemorrhage, subarachnoid hemorrhage, or intraventricular hemorrhage that is the predominant cause of ≥4 point NIHSS deterioration at 24 hours.

Secondary Outcome Measures

modified Rankin Scale (mRS) score of ≤2
modified Ranking Scale is a commonly used scale for measuring the degree of disability or dependence in the daily activities of people who have suffered a stroke. The scale runs from 0-6, running from perfect health without symptoms to death.

Full Information

First Posted
March 6, 2018
Last Updated
July 20, 2020
Sponsor
Rapid Medical
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1. Study Identification

Unique Protocol Identification Number
NCT03474549
Brief Title
Treatment With Intent to Generate Endovascular Reperfusion
Acronym
TIGER
Official Title
Treatment With Intent to Generate Endovascular Reperfusion
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
May 9, 2018 (Actual)
Primary Completion Date
April 15, 2020 (Actual)
Study Completion Date
June 30, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Rapid Medical

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Device Product Not Approved or Cleared by U.S. FDA
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Tigertriever is a CE marked mechanical revascularization device indicated to restore blood flow by removing thrombus from a large intracranial vessel in patients experiencing ischemic stroke within 8 hours of symptom onset. Patients who are ineligible for IV t-PA or who fail IV t-PA therapy are candidates for treatment. The objective of the TIGER Study is to evaluate the safety and effectiveness of the Tigertriever device in restoring blood flow in the neurovasculature by removing thrombus in patients experiencing ischemic stroke due to a large vessel occlusion (LVO). This study is designed to support substantial equivalence to approved and marketed products such as the Solitaire or Trevo Retriever.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ischemic Stroke
Keywords
Mechanical thrombectomy,, Brain, Brain clot, Brain infarction, Cerebral ischemia, Neurovascular intervention, Revascularization, Reperfusion, Stent retriever, Tigertriever, Stroke, Rapid Medical

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
160 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tigertriever revascularization device
Arm Type
Experimental
Arm Description
Mechanical thrombectomy with Tigertriever
Intervention Type
Device
Intervention Name(s)
Tigertriever revascularization device
Intervention Description
Mechanical Thrombectomy
Primary Outcome Measure Information:
Title
Successful reperfusion, defined as mTICI Score ≥ 2b
Description
Effectiveness (Successful reperfusion)
Time Frame
Day 0 (end of procedure)
Title
All-cause mortality
Description
Safety (All-cause mortality)
Time Frame
90 days post treatment
Title
Symptomatic intracranial hemorrhage (sICH) defined as any parenchymal hematoma type 2, remote intracerebral hemorrhage, subarachnoid hemorrhage, or intraventricular hemorrhage that is the predominant cause of ≥4 point NIHSS deterioration at 24 hours
Description
Safety (Symptomatic intracranial hemorrhage (sICH)) defined as any parenchymal hematoma type 2, remote intracerebral hemorrhage, subarachnoid hemorrhage, or intraventricular hemorrhage that is the predominant cause of ≥4 point NIHSS deterioration at 24 hours.
Time Frame
24 hours post procedure
Secondary Outcome Measure Information:
Title
modified Rankin Scale (mRS) score of ≤2
Description
modified Ranking Scale is a commonly used scale for measuring the degree of disability or dependence in the daily activities of people who have suffered a stroke. The scale runs from 0-6, running from perfect health without symptoms to death.
Time Frame
90 days post 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: New focal neurologic deficit consistent with being of acute cerebral ischemia origin. Age 18-85 years old (inclusive). Interventionalist estimates that treatment with the Tigertriever (first deployment in target vessel) can be achieved within 8 hours of symptom onset. Patient either: a) eligible for, and received, IV t-PA within 3 hours of symptom onset, at the correct 0.9 mg/kg dose, or b) ineligible for IV t-PA. NIH Stroke Scale score of 8-29. No known significant pre-stroke disability (prestroke mRS 0 or 1). Catheter angiographic confirmation of a large vessel occlusion in the intracranial internal carotid artery, the M1 or M2 segments of the middle cerebral artery, the intracranial vertebral artery, or the basilar artery that is accessible to Tigertriever device. For strokes in the anterior circulation, the following imaging criteria should also be met: MRI criterion: volume of diffusion restriction visually assessed ≤50 mL, OR CT criterion: ASPECTS 6 to 10 on baseline NCCT or CTA-source images, For strokes in the posterior circulation, the following imaging criterion should also be met: pcASPECTS score 8 to 10 on baseline NCCT, CTA-source images, or DWI MRI. Anticipated life expectancy of at least 6 months. A signed informed consent by patient or a Legally Authorized Representative or independent physician in case of oral consent. Exclusion Criteria: Subject already participating in another study of an investigational treatment device or treatment. Use of any other intra-arterial recanalization drug or device prior to the Tigertriever (Tigertriever not as first choice device). Angiographically evident excessive arterial tortuosity precluding device access to the thrombus. For all patients, severe sustained hypertension with SBP >220 and/or DBP >120; for patients treated with IV tPA, sustained hypertension despite treatment with SBP >185 and/or DBP > 110. Glucose < 50 mg/dl (2.78 mmol/L) or > 400 mg/dl (22.20 mmol/L). Known hemorrhagic diathesis. Coagulation factor deficiency or oral anti-coagulant therapy with an international normalized ratio (INR) of more than 3.0. Treatment with heparin within 48 h with a partial thromboplastin time more than two times the laboratory normal. Patients who have received a direct thrombin inhibitor within the last 48 hours; must have a partial thromboplastin time (PTT) less than 1.5 times the normal to be eligible. Platelet count of less than 50,000/uL. History of severe allergy to contrast medium, nickel, or Nitinol. Intracranial hemorrhage. Significant mass effect with midline shift. Intracranial tumor (apart from small meningioma, ≤ 2 cm in diameter). Stenosis or any occlusion in the deployment site or in a proximal vessel requiring treatment or preventing device access to the thrombus (for example, stenosis or occlusion in the cervical internal carotid artery). Females who are pregnant or breastfeeding. Known current use of cocaine at time of treatment. Prior recent stroke in the past 3 months. Renal failure with serum creatinine >3.0 or Glomerular Filtration Rate (GFR) <30. Known cerebral vasculitis. Rapidly improving neurological status defined as improvement of greater than 8 points on the NIHSS or improvement to NIHSS of < 6 prior to procedure Clinical symptoms suggestive of bilateral stroke or stroke in multiple territories. Ongoing seizure due to stroke. Evidence of active systemic infection. Known cancer with metastases. Suspicion of aortic dissection, septic embolus, or bacterial endocarditis. Evidence of dissection in the extra or intracranial cerebral arteries. Occlusions in multiple vascular territories (e.g., bilateral anterior circulation, or anterior/posterior circulation). Aneurysm in target vessel.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeffrey L Saver, Dr.
Organizational Affiliation
Geffen School of Medicine at UCLA
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Rishi Gupta, Dr.
Organizational Affiliation
WellStar Medical Group
Official's Role
Principal Investigator
Facility Information:
Facility Name
UCLA medical center
City
Los Angeles
State/Province
California
ZIP/Postal Code
90095
Country
United States
Facility Name
Los Robles
City
Thousand Oaks
State/Province
California
ZIP/Postal Code
91360
Country
United States
Facility Name
Tenet Health
City
Coral Springs
State/Province
Florida
ZIP/Postal Code
33076
Country
United States
Facility Name
Baptist Health Research Institute
City
Jacksonville
State/Province
Florida
ZIP/Postal Code
32207
Country
United States
Facility Name
Baptist Health South Florida
City
Miami
State/Province
Florida
ZIP/Postal Code
33176
Country
United States
Facility Name
University of Miami
City
Miami
State/Province
Florida
ZIP/Postal Code
33316
Country
United States
Facility Name
WellStar Research Institute
City
Marietta
State/Province
Georgia
ZIP/Postal Code
30060
Country
United States
Facility Name
University of Iowa
City
Iowa City
State/Province
Iowa
ZIP/Postal Code
52242
Country
United States
Facility Name
University of Massachusetts
City
Worcester
State/Province
Massachusetts
ZIP/Postal Code
01655
Country
United States
Facility Name
Maimonides Medical Center
City
Brooklyn
State/Province
New York
ZIP/Postal Code
11219
Country
United States
Facility Name
University of Buffalo
City
Buffalo
State/Province
New York
ZIP/Postal Code
14203
Country
United States
Facility Name
Riverside Methodist Hospital
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43214
Country
United States
Facility Name
Mercy Health
City
Toledo
State/Province
Ohio
ZIP/Postal Code
43604
Country
United States
Facility Name
Oregon Health & Science University
City
Portland
State/Province
Oregon
ZIP/Postal Code
97239
Country
United States
Facility Name
UPMC
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States
Facility Name
VBMC Harlingen
City
Harlingen
State/Province
Texas
ZIP/Postal Code
78550
Country
United States
Facility Name
Rambam
City
Haifa
Country
Israel

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33739136
Citation
Gupta R, Saver JL, Levy E, Zaidat OO, Yavagal D, Liebeskind DS, Khaldi A, Gross B, Lang M, Narayanan S, Jankowitz B, Snyder K, Siddiqui A, Davies J, Lin E, Hassan A, Hanel R, Aghaebrahim A, Kaushal R, Malek A, Mueller-Kronast N, Starke R, Bozorgchami H, Nesbit G, Horikawa M, Priest R, Liu J, Budzik RF, Pema P, Vora N, Taqi MA, Samaniego E, Wang QT, Nossek E, Dabus G, Linfante I, Puri A, Abergel E, Starkman S, Tateshima S, Jadhav AP; TIGER Trial Investigators. New Class of Radially Adjustable Stentrievers for Acute Ischemic Stroke: Primary Results of the Multicenter TIGER Trial. Stroke. 2021 May;52(5):1534-1544. doi: 10.1161/STROKEAHA.121.034436. Epub 2021 Mar 19. Erratum In: Stroke. 2021 Jun;52(6):e310.
Results Reference
derived

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Treatment With Intent to Generate Endovascular Reperfusion

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