Brief Summary
The trial is designed to assess the safety and efficacy of using the Zoom Reperfusion System in subjects diagnosed with acute ischemic stroke and undergoing a thrombectomy procedure within 8 hours of last known well.
Brief Title
The Imperative Trial: Treatment of Acute Ischemic Stroke With the Zoom Reperfusion System
Detailed Description
Each year 17 million people suffer stroke worldwide. According to the World Stroke Organization, stroke has become the second cause of death and disability worldwide. In the United States, every year, more than 795,000 people have a stroke. Given the large-scale challenges of curing stroke, prevention and treatments for stroke are much needed. Ischemic stroke is treatable in many patients if they have early access to viable treatments.
This trial is a prospective, multicenter, open-label, single-arm trial designed to assess the potential treatment benefits of using the Imperative Care 0.088" Catheters in conjunction with the other devices in the Zoom Reperfusion System to restore blood flow in patients with acute ischemic stroke secondary to intracranial large vessel occlusive disease. The Zoom Reperfusion System includes the Imperative Care 0.088" Catheters, the Zoom Reperfusion Catheters (0.035" to 0.071" Catheters), Zoom Aspiration Tubing, and Zoom Aspiration Pump. The trial will assess reperfusion success using the mTICI scores in the absence of any rescue therapy, reperfusion time, first-pass success, and functional independence including a quality-of-life assessment.
This trial is a prospective, multicenter, open-label, single-arm trial designed to assess the potential treatment benefits of using the Imperative Care 0.088" Catheters in conjunction with the other devices in the Zoom Reperfusion System to restore blood flow in patients with acute ischemic stroke secondary to intracranial large vessel occlusive disease. The Zoom Reperfusion System includes the Imperative Care 0.088" Catheters, the Zoom Reperfusion Catheters (0.035" to 0.071" Catheters), Zoom Aspiration Tubing, and Zoom Aspiration Pump. The trial will assess reperfusion success using the mTICI scores in the absence of any rescue therapy, reperfusion time, first-pass success, and functional independence including a quality-of-life assessment.
Categories
Completion Date
Completion Date Type
Actual
Conditions
Ischemic Stroke
Acute Stroke
Eligibility Criteria
Inclusion Criteria:
1. Age 18 and older
2. NIHSS \>=6
3. The operator feels that the stroke can be treated with endovascular thrombectomy approaches and the interventionalist estimates that groin puncture can be achieved within 8 hours from time last seen well
4. Pre-event mRS scale 0-1
5. Large vessel occlusion of the intracranial internal carotid artery (ICA), middle cerebral artery (MCA)-M1 or M2 segments, basilar, or vertebral arteries as evidenced by MRA or CTA
6. For strokes in anterior circulation, ASPECTS \>=6; For strokes in posterior circulation, pc-ASPECTS \>=8
7. Non-contrast CT/CTA or MRI/MRA for trial eligibility performed or repeated at treating stroke center or outside medical facility within 2 hours of treatment initiation
8. If indicated per American Heart Association clinical guidelines, thrombolytic therapy should be administered as soon as possible
9. Consenting requirements met according to local IRB or Ethics Committee
Exclusion Criteria:
1. Female known to be pregnant at time of admission
2. Patient has suffered a stroke in the past 3 months
3. Presence of an existing or pre-existing large territory infarction
4. Pre-existing neurological or psychiatric disease that would confound the neurological or functional evaluation, e.g., dementia with prescribed anti-cholinesterase inhibitor
5. Known history of severe contrast allergy or absolute contraindication to iodinated contrast
6. Clinical history, past imaging or clinical judgement suggest that the intracranial occlusion is chronic
7. Life expectancy of less than 6 months prior to stroke onset
8. Clinical symptoms suggestive of bilateral stroke or stroke in multiple territories
9. Subject participating in another clinical trial involving an investigational device or drug
10. Known cancer with metastases
11. Evidence of active systemic infection
12. Any known hemorrhagic or coagulation deficiency
Imaging Exclusion Criteria:
13. Evidence of intracranial hemorrhage on CT/MRI
14. CTA or MRA evidence of carotid stenosis requiring treatment for intracranial access
15. Excessive vascular access tortuosity or target vessel size that will likely prevent endovascular access with the Imperative Care 0.088" ID Catheters
16. Intracranial stent implanted in the same vascular territory that would preclude the safe deployment/removal of the thrombectomy devices
17. Occlusions in multiple vascular territories (e.g., bilateral anterior circulation, or anterior circulation/vertebrobasilar system) as confirmed on CTA/MRA, or clinical evidence of bilateral strokes or strokes in multiple territories as determined by the treating physician
18. Significant mass effect with midline shift as confirmed on CT/MRI
19. Evidence of intracranial tumor (except small meningioma defined as ≤ 3cm and asymptomatic) as confirmed on CT/MRI
20. Angiographic evidence of pre-existing arterial injury, e.g., carotid dissection, complete cervical carotid occlusion, or vasculitis
1. Age 18 and older
2. NIHSS \>=6
3. The operator feels that the stroke can be treated with endovascular thrombectomy approaches and the interventionalist estimates that groin puncture can be achieved within 8 hours from time last seen well
4. Pre-event mRS scale 0-1
5. Large vessel occlusion of the intracranial internal carotid artery (ICA), middle cerebral artery (MCA)-M1 or M2 segments, basilar, or vertebral arteries as evidenced by MRA or CTA
6. For strokes in anterior circulation, ASPECTS \>=6; For strokes in posterior circulation, pc-ASPECTS \>=8
7. Non-contrast CT/CTA or MRI/MRA for trial eligibility performed or repeated at treating stroke center or outside medical facility within 2 hours of treatment initiation
8. If indicated per American Heart Association clinical guidelines, thrombolytic therapy should be administered as soon as possible
9. Consenting requirements met according to local IRB or Ethics Committee
Exclusion Criteria:
1. Female known to be pregnant at time of admission
2. Patient has suffered a stroke in the past 3 months
3. Presence of an existing or pre-existing large territory infarction
4. Pre-existing neurological or psychiatric disease that would confound the neurological or functional evaluation, e.g., dementia with prescribed anti-cholinesterase inhibitor
5. Known history of severe contrast allergy or absolute contraindication to iodinated contrast
6. Clinical history, past imaging or clinical judgement suggest that the intracranial occlusion is chronic
7. Life expectancy of less than 6 months prior to stroke onset
8. Clinical symptoms suggestive of bilateral stroke or stroke in multiple territories
9. Subject participating in another clinical trial involving an investigational device or drug
10. Known cancer with metastases
11. Evidence of active systemic infection
12. Any known hemorrhagic or coagulation deficiency
Imaging Exclusion Criteria:
13. Evidence of intracranial hemorrhage on CT/MRI
14. CTA or MRA evidence of carotid stenosis requiring treatment for intracranial access
15. Excessive vascular access tortuosity or target vessel size that will likely prevent endovascular access with the Imperative Care 0.088" ID Catheters
16. Intracranial stent implanted in the same vascular territory that would preclude the safe deployment/removal of the thrombectomy devices
17. Occlusions in multiple vascular territories (e.g., bilateral anterior circulation, or anterior circulation/vertebrobasilar system) as confirmed on CTA/MRA, or clinical evidence of bilateral strokes or strokes in multiple territories as determined by the treating physician
18. Significant mass effect with midline shift as confirmed on CT/MRI
19. Evidence of intracranial tumor (except small meningioma defined as ≤ 3cm and asymptomatic) as confirmed on CT/MRI
20. Angiographic evidence of pre-existing arterial injury, e.g., carotid dissection, complete cervical carotid occlusion, or vasculitis
Inclusion Criteria
Inclusion Criteria:
1. Age 18 and older
2. NIHSS \>=6
3. The operator feels that the stroke can be treated with endovascular thrombectomy approaches and the interventionalist estimates that groin puncture can be achieved within 8 hours from time last seen well
4. Pre-event mRS scale 0-1
5. Large vessel occlusion of the intracranial internal carotid artery (ICA), middle cerebral artery (MCA)-M1 or M2 segments, basilar, or vertebral arteries as evidenced by MRA or CTA
6. For strokes in anterior circulation, ASPECTS \>=6; For strokes in posterior circulation, pc-ASPECTS \>=8
7. Non-contrast CT/CTA or MRI/MRA for trial eligibility performed or repeated at treating stroke center or outside medical facility within 2 hours of treatment initiation
8. If indicated per American Heart Association clinical guidelines, thrombolytic therapy should be administered as soon as possible
9. Consenting requirements met according to local IRB or Ethics Committee
1. Age 18 and older
2. NIHSS \>=6
3. The operator feels that the stroke can be treated with endovascular thrombectomy approaches and the interventionalist estimates that groin puncture can be achieved within 8 hours from time last seen well
4. Pre-event mRS scale 0-1
5. Large vessel occlusion of the intracranial internal carotid artery (ICA), middle cerebral artery (MCA)-M1 or M2 segments, basilar, or vertebral arteries as evidenced by MRA or CTA
6. For strokes in anterior circulation, ASPECTS \>=6; For strokes in posterior circulation, pc-ASPECTS \>=8
7. Non-contrast CT/CTA or MRI/MRA for trial eligibility performed or repeated at treating stroke center or outside medical facility within 2 hours of treatment initiation
8. If indicated per American Heart Association clinical guidelines, thrombolytic therapy should be administered as soon as possible
9. Consenting requirements met according to local IRB or Ethics Committee
Gender
All
Gender Based
false
Keywords
stroke, thrombectomy, Zoom, aspiration, reperfusion, mRS
Healthy Volunteers
No
Last Update Post Date
Last Update Post Date Type
Actual
Last Update Submit Date
Minimum Age
18 Years
NCT Id
NCT04129125
Org Class
Industry
Org Full Name
Imperative Care, Inc.
Org Study Id
ICI-001
Overall Status
Completed
Phases
Not Applicable
Primary Completion Date
Primary Completion Date Type
Actual
Official Title
A Prospective, Multi-center, Open Label and Single Arm Clinical Investigation to Evaluate the Safety and Efficacy of Using the Zoom Reperfusion System in Thrombectomy Procedures to Treat Acute Ischemic Stroke Patients
Primary Outcomes
Outcome Description
Reperfusion success was defined as achieving a modified Treatment in Cerebral Infarction (mTICI) score of ≥2b within three or fewer passes using the study device and without rescue therapy (e.g., additional thrombectomy devices or intra-arterial lytics). The mTICI scale ranges from 0 to 3, with higher scores indicating better reperfusion: 0 = no perfusion, 1 = minimal perfusion, 2a = partial (\<50%), 2b = substantial (≥50%), 2c = near complete, 3 = complete. This measure reports the number of participants who achieved mTICI ≥2b under these criteria as adjudicated by an independent core lab.
Outcome Measure
ITT Cohort: Rate of Core Lab-adjudicated Reperfusion Success
Outcome Time Frame
Intraprocedural
Outcome Description
Rate of symptomatic intracranial hemorrhage (sICH), as independently adjudicated by the core lab and the independent safety board
Outcome Measure
ITT Cohort: Rate of Symptomatic Intracranial Hemorrhage (sICH), as Independently Adjudicated by Core Lab and Safety Board
Outcome Time Frame
24-hour post-procedure
Outcome Description
Reperfusion success was defined as achieving a modified Treatment in Cerebral Infarction (mTICI) score of ≥2b within three or fewer passes using the study device and without rescue therapy (e.g., additional thrombectomy devices or intra-arterial lytics). The mTICI scale ranges from 0 to 3, with higher scores indicating better reperfusion: 0 = no perfusion, 1 = minimal perfusion, 2a = partial (\<50%), 2b = substantial (≥50%), 2c = near complete, 3 = complete. This measure reports the number of participants who achieved mTICI ≥2b under these criteria as adjudicated by an independent core lab.
Outcome Measure
FDA Clearance Cohort: Rate of Core Lab-adjudicated Reperfusion Success
Outcome Time Frame
Intraprocedural
Outcome Description
Rate of symptomatic intracranial hemorrhage (sICH), as independently adjudicated by the core lab and the independent safety board
Outcome Measure
FDA Clearance Cohort: Rate of Symptomatic Intracranial Hemorrhage (sICH), as Independently Adjudicated by Core Lab and Safety Board
Outcome Time Frame
24-hour post-procedure
Outcome Description
Reperfusion success was defined as achieving a modified Treatment in Cerebral Infarction (mTICI) score of ≥2b within three or fewer passes using the study device and without rescue therapy (e.g., additional thrombectomy devices or intra-arterial lytics). The mTICI scale ranges from 0 to 3, with higher scores indicating better reperfusion: 0 = no perfusion, 1 = minimal perfusion, 2a = partial (\<50%), 2b = substantial (≥50%), 2c = near complete, 3 = complete. This measure reports the number of participants who achieved mTICI ≥2b under these criteria as adjudicated by an independent core lab.
Outcome Measure
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of Core Lab-adjudicated Reperfusion Success
Outcome Time Frame
Intraprocedural
Outcome Description
Rate of symptomatic intracranial hemorrhage (sICH), as independently adjudicated by the core lab and the independent safety board
Outcome Measure
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of Symptomatic Intracranial Hemorrhage (sICH), as Independently Adjudicated by Core Lab and Safety Board
Outcome Time Frame
24-hour post-procedure
Secondary Outcomes
Outcome Description
The time from groin puncture to mTICI (modified treatment in cerebral infarction) score ≥ 2b
mTICI range: 0 to 3; higher score means better reperfusion
mTICI range: 0 to 3; higher score means better reperfusion
Outcome Time Frame
Intraprocedural
Outcome Measure
ITT Cohort: Time to Achieve mTICI Score ≥ 2b
Outcome Description
Independent core lab-adjudicated reperfusion success, defined as modified treatment in cerebral infarction (mTICI) score = 3 within three or fewer passes with the study device, without using rescue therapy (e.g., additional thrombectomy devices or intra-arterial lytics)
mTICI range: 0 to 3; higher score means better reperfusion
mTICI range: 0 to 3; higher score means better reperfusion
Outcome Time Frame
Intraprocedural
Outcome Measure
ITT Cohort: Rate of mTICI Score 3 Reperfusion
Outcome Description
Independent core lab-adjudicated modified treatment in cerebral infarction (mTICI) score ≥2b after the first pass with the study device
mTICI range: 0 to 3; higher score means better outcome
mTICI range: 0 to 3; higher score means better outcome
Outcome Time Frame
Intraprocedural
Outcome Measure
ITT Cohort: Rate of First Pass Success
Outcome Description
Independent core lab-adjudicated reperfusion success, defined as modified treatment in cerebral infarction (mTICI) score ≥2c within three or fewer passes with the study device, without using rescue therapy (e.g., additional thrombectomy devices or intra-arterial lytics)
mTICI range: 0 to 3; higher score means better outcome
mTICI range: 0 to 3; higher score means better outcome
Outcome Time Frame
Intraprocedural
Outcome Measure
ITT Cohort: Rate of mTICI Score 2c Reperfusion
Outcome Description
The proportion of patients achieving modified Rankin Scale (mRS) score ≤2 using the primary treatment modality, evaluated by certified assessors
The mRS scale ranges from 0 (no symptoms) to 5 (severe disability), with an additional category of 6 for death
The mRS scale ranges from 0 (no symptoms) to 5 (severe disability), with an additional category of 6 for death
Outcome Time Frame
90-days post-procedure
Outcome Measure
ITT Cohort: Rate of Functional Independence
Outcome Description
The Stroke Impact Scale (SIS) is a self-reported questionnaire assessing quality of life in 8 domains: Strength, Memory and Thinking, Emotion, Communication, ADL/IADL, Mobility, Hand Function, and Participation/Role Function. Each domain is scored from 0 to 100, with higher scores indicating better function and less impact of stroke. Scores are calculated by averaging item responses in each domain and transforming to a 0-100 scale. A separate recovery score from 0 (no recovery) to 100 (full recovery) reflects the patient's overall perception of recovery. Domain scores are not combined into a total score.
Outcome Time Frame
90 days post-procedure
Outcome Measure
ITT Cohort: Quality of Life Assessment
Outcome Description
Rate of 90-day all-cause mortality
Outcome Time Frame
90 days post-procedure
Outcome Measure
ITT Cohort: Rate of All-Cause Mortality
Outcome Description
Independent core lab adjudicated rate of all ICH at 24-hour post-procedure
Outcome Time Frame
24-hour post-procedure
Outcome Measure
ITT Cohort: Rate of All Intracranial Hemorrhage (ICH)
Outcome Description
Rate of participants with embolism into a new territory (ENT) as evidenced by new occlusions noted post-procedure or new infarcts identified on 24-hour imaging that are remote to the vascular territory impacted by the index stroke
Outcome Time Frame
24-hour post-procedure
Outcome Measure
ITT Cohort: Rate of Embolization in New Territory (ENT)
Outcome Description
Independent Safety Board adjudicated device-related serious adverse device events within 90 days post-procedure
Outcome Time Frame
90 days post-procedure
Outcome Measure
ITT Cohort: Rate of Serious Adverse Device Effects (SADEs)
Outcome Description
All serious adverse events through 90 days post-procedure.
Outcome Time Frame
90 days post-procedure
Outcome Measure
ITT Cohort: Rate of Serious Adverse Events
Outcome Description
The time from groin puncture to mTICI (modified treatment in cerebral infarction) score ≥ 2b
mTICI range: 0 to 3; higher score means better reperfusion
mTICI range: 0 to 3; higher score means better reperfusion
Outcome Time Frame
Intraprocedural
Outcome Measure
FDA Clearance Cohort: Time to Achieve mTICI Score ≥ 2b
Outcome Description
Independent core lab-adjudicated reperfusion success, defined as modified treatment in cerebral infarction (mTICI) score = 3 within three or fewer passes with the study device, without using rescue therapy (e.g., additional thrombectomy devices or intra-arterial lytics)
mTICI range: 0 to 3; higher score means better outcome
mTICI range: 0 to 3; higher score means better outcome
Outcome Time Frame
Intraprocedural
Outcome Measure
FDA Clearance Cohort: Rate of mTICI Score 3 Reperfusion
Outcome Description
Independent core lab-adjudicated modified treatment in cerebral infarction (mTICI) score ≥2b after the first pass with the study device
mTICI range: 0 to 3; higher score means better outcome
mTICI range: 0 to 3; higher score means better outcome
Outcome Time Frame
Intraprocedural
Outcome Measure
FDA Clearance Cohort: Rate of First Pass Success
Outcome Description
Independent core lab-adjudicated reperfusion success, defined as modified treatment in cerebral infarction (mTICI) score ≥2c within three or fewer passes with the study device, without using rescue therapy (e.g., additional thrombectomy devices or intra-arterial lytics)
mTICI range: 0 to 3; higher score means better reperfusion
mTICI range: 0 to 3; higher score means better reperfusion
Outcome Time Frame
Intraprocedural
Outcome Measure
FDA Clearance Cohort: Rate of mTICI Score 2c Reperfusion
Outcome Description
The proportion of patients achieving modified Rankin Scale (mRS) score ≤2 using the primary treatment modality, evaluated by certified assessors
The mRS scale ranges from 0 (no symptoms) to 5 (severe disability), with an additional category of 6 for death.
The mRS scale ranges from 0 (no symptoms) to 5 (severe disability), with an additional category of 6 for death.
Outcome Time Frame
90-days post-procedure
Outcome Measure
FDA Clearance Cohort: Rate of Functional Independence
Outcome Description
The Stroke Impact Scale (SIS) is a self-reported questionnaire assessing quality of life in 8 domains: Strength, Memory and Thinking, Emotion, Communication, ADL/IADL, Mobility, Hand Function, and Participation/Role Function. Each domain is scored from 0 to 100, with higher scores indicating better function and less impact of stroke. Scores are calculated by averaging item responses in each domain and transforming to a 0-100 scale. A separate recovery score from 0 (no recovery) to 100 (full recovery) reflects the patient's overall perception of recovery. Domain scores are not combined into a total score.
Outcome Time Frame
90-days post-procedure
Outcome Measure
FDA Clearance Cohort: Quality of Life Assessment
Outcome Description
Rate of 90-day all-cause mortality
Outcome Time Frame
90-days post-procedure
Outcome Measure
FDA Clearance Cohort: Rate of All-Cause Mortality
Outcome Description
Independent core lab adjudicated rate of all ICH at 24-hour post-procedure
Outcome Time Frame
24-hour post-procedure
Outcome Measure
FDA Clearance Cohort: Rate of All Intracranial Hemorrhage (ICH)
Outcome Description
Rate of participants with embolism into a new territory (ENT) as evidenced by new occlusions noted post-procedure or new infarcts identified on 24-hour imaging that are remote to the vascular territory impacted by the index stroke
Outcome Time Frame
End of procedure to 24-hour post-procedure
Outcome Measure
FDA Clearance Cohort: Rate of Embolization in New Territory (ENT)
Outcome Description
Independent Safety Board adjudicated device-related serious adverse device events within 90 days post-procedure
Outcome Time Frame
90-days post-procedure
Outcome Measure
FDA Clearance Cohort: Rate of Serious Adverse Device Effects (SADEs)
Outcome Description
All serious adverse events through 90 days post-procedure.
Outcome Time Frame
90-days post-procedure
Outcome Measure
FDA Clearance Cohort: Rate of Serious Adverse Events
Outcome Description
The time from groin puncture to mTICI (modified treatment in cerebral infarction) score ≥ 2b flow.
mTICI range: 0 to 3; higher score means better reperfusion
mTICI range: 0 to 3; higher score means better reperfusion
Outcome Time Frame
Intraprocedural
Outcome Measure
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Time to Achieve mTICI Score ≥ 2b
Outcome Description
Independent core lab-adjudicated reperfusion success, defined as modified treatment in cerebral infarction (mTICI) score = 3 within three or fewer passes with the study device, without using rescue therapy (e.g., additional thrombectomy devices or intra-arterial lytics)
mTICI range: 0 to 3; higher score means better reperfusion
mTICI range: 0 to 3; higher score means better reperfusion
Outcome Time Frame
Intraprocedural
Outcome Measure
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of mTICI Score 3 Reperfusion
Outcome Description
Independent core lab-adjudicated modified treatment in cerebral infarction (mTICI) score ≥2b after the first pass with the study device
mTICI range: 0 to 3; higher score means better reperfusion
mTICI range: 0 to 3; higher score means better reperfusion
Outcome Time Frame
Intraprocedural
Outcome Measure
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of First Pass Success
Outcome Description
Independent core lab-adjudicated reperfusion success, defined as modified treatment in cerebral infarction (mTICI) score ≥2c within three or fewer passes with the study device, without using rescue therapy (e.g., additional thrombectomy devices or intra-arterial lytics)
mTICI range: 0 to 3; higher score means better reperfusion
mTICI range: 0 to 3; higher score means better reperfusion
Outcome Time Frame
Intraprocedural
Outcome Measure
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of mTICI Score 2c Reperfusion
Outcome Description
The proportion of patients achieving modified Rankin Scale (mRS) score ≤2 using the primary treatment modality, evaluated by certified assessors
The mRS scale ranges from 0 (no symptoms) to 5 (severe disability), with an additional category of 6 for death.
The mRS scale ranges from 0 (no symptoms) to 5 (severe disability), with an additional category of 6 for death.
Outcome Time Frame
90-days post-procedure
Outcome Measure
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of Functional Independence
Outcome Description
The Stroke Impact Scale (SIS) is a self-reported questionnaire assessing quality of life in 8 domains: Strength, Memory and Thinking, Emotion, Communication, ADL/IADL, Mobility, Hand Function, and Participation/Role Function. Each domain is scored from 0 to 100, with higher scores indicating better function and less impact of stroke. Scores are calculated by averaging item responses in each domain and transforming to a 0-100 scale. A separate recovery score from 0 (no recovery) to 100 (full recovery) reflects the patient's overall perception of recovery. Domain scores are not combined into a total score.
Outcome Time Frame
90-days post-procedure
Outcome Measure
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Quality of Life Assessment
Outcome Description
Rate of 90-day all-cause mortality
Outcome Time Frame
90-days post-procedure
Outcome Measure
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of All-Cause Mortality
Outcome Description
Independent core lab adjudicated rate of all ICH at 24-hour post-procedure
Outcome Time Frame
24-hour post-procedure
Outcome Measure
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of All Intracranial Hemorrhage (ICH)
Outcome Description
Rate of participants with embolism into a new territory (ENT) as evidenced by new occlusions noted post-procedure or new infarcts identified on 24-hour imaging that are remote to the vascular territory impacted by the index stroke
Outcome Time Frame
End of procedure to 24-hour post-procedure
Outcome Measure
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of Embolization in New Territory (ENT)
Outcome Description
Independent Safety Board adjudicated device-related serious adverse device events within 90 days post-procedure
Outcome Time Frame
90-days post-procedure
Outcome Measure
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of Serious Adverse Device Effects (SADEs)
Outcome Description
All serious adverse events through 90 days post-procedure
Outcome Time Frame
90-days post-procedure
Outcome Measure
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of Serious Adverse Events
Start Date
Start Date Type
Actual
Status Verified Date
First Post Date
First Post Date Type
Actual
First Submit Date
First Submit QC Date
Std Ages
Adult
Older Adult
Maximum Age Number (converted to Years and rounded down)
999
Minimum Age Number (converted to Years and rounded down)
18
Investigators
Investigator Type
Principal Investigator
Investigator Name
Neil Haranhalli
Investigator Email
nharanha@montefiore.org
Investigator Phone
NHARANHA
Categories Mesh Debug
Brain, Spinal Cord & Nervous System --- ISCHEMIC STROKE
Brain, Spinal Cord & Nervous System --- STROKE
Brain, Spinal Cord & Nervous System --- CEREBROVASCULAR DISORDERS
Alzheimer's --- BRAIN DISEASES
Brain, Spinal Cord & Nervous System --- BRAIN DISEASES
Brain, Spine & Nerve Cancers --- BRAIN DISEASES
Alzheimer's --- CENTRAL NERVOUS SYSTEM DISEASES
Brain, Spinal Cord & Nervous System --- CENTRAL NERVOUS SYSTEM DISEASES
Brain, Spine & Nerve Cancers --- CENTRAL NERVOUS SYSTEM DISEASES
Brain, Spinal Cord & Nervous System --- NERVOUS SYSTEM DISEASES
Brain, Spine & Nerve Cancers --- NERVOUS SYSTEM DISEASES
Blood & Bone Marrow Cancers --- VASCULAR DISEASES
Heart/Cardiovascular --- VASCULAR DISEASES
Blood Disorders --- CARDIOVASCULAR DISEASES
Blood & Bone Marrow Cancers --- CARDIOVASCULAR DISEASES
Heart/Cardiovascular --- CARDIOVASCULAR DISEASES
MeSH Terms
ISCHEMIC STROKE
STROKE
CEREBROVASCULAR DISORDERS
BRAIN DISEASES
CENTRAL NERVOUS SYSTEM DISEASES
NERVOUS SYSTEM DISEASES
VASCULAR DISEASES
CARDIOVASCULAR DISEASES