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The Imperative Trial: Treatment of Acute Ischemic Stroke With the Zoom Reperfusion System

Primary Purpose

Ischemic Stroke, Acute Stroke

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Zoom Reperfusion System
Sponsored by
Imperative Care, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ischemic Stroke focused on measuring stroke, thrombectomy, Zoom, aspiration, reperfusion, mRS

Eligibility Criteria

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

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, IV t-PA should be administered as soon as possible, but no later than 3 hours from onset of stroke symptoms (onset time is defined as the last time when the patient was witnessed to be at baseline)
  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

Sites / Locations

  • Radiology of HuntsvilleRecruiting
  • Carondelet Neurological Institute St. Joseph's HospitalRecruiting
  • University of Southern CaliforniaRecruiting
  • John Muir HealthRecruiting
  • Baptist HealthRecruiting
  • University of Miami / Jackson Memorial HospitalRecruiting
  • Tallahassee Neurological ClinicRecruiting
  • Tampa General Hospital / University of South FloridaRecruiting
  • Grady Memorial Hospital / Emory UniversityRecruiting
  • Ochsner HealthRecruiting
  • Spectrum HealthRecruiting
  • Munson Medical CenterRecruiting
  • Cooper University Health CareRecruiting
  • Montefiore Medical CenterRecruiting
  • The State University of New York at BuffaloRecruiting
  • Mount SinaiRecruiting
  • The Ohio State University Medical CenterRecruiting
  • Oklahoma UniversityRecruiting
  • Lehigh Valley HospitalRecruiting
  • University of PennsylvaniaRecruiting
  • Prisma Health - UpstateRecruiting
  • Erlanger Health System: Tennessee Interventional and Imaging AssociatesRecruiting
  • Semmes Murphey Foundation / Methodist University HospitalRecruiting
  • Baylor Scott and White Research InstituteRecruiting
  • Valley Baptist Medical CenterRecruiting
  • The University of Texas Health Science Center at Houston // Memorial Hermann Health SystemRecruiting
  • University of Texas Health Science Center at San AntonioRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Zoom Reperfusion System

Arm Description

The subject will undergo the endovascular thrombectomy procedure under general anesthesia or conscious sedation. The Imperative Care .088" Catheter will be used to gain access to the vasculature and direct aspiration of the clot will be attempted where feasible. The Zoom Reperfusion System must be the initial and primary device used to remove thrombus.

Outcomes

Primary Outcome Measures

Primary Efficacy Endpoint
Rate of reperfusion success, defined as achieving mTICI score ≥ 2b flow with the Zoom Reperfusion System (primary treatment modality) without using additional thrombectomy devices or rescue therapy.
Primary Safety Endpoint
Rate of symptomatic intracranial hemorrhage (sICH), as confirmed by imaging

Secondary Outcome Measures

Time to achieve mTICI score ≥ 2b
The time from groin puncture to mTICI score ≥ 2b flow
Rate of mTICI score 3 reperfusion
The proportion of patients achieving mTICI score 3 flow
First pass success
The proportion of patients where the mTICI score ≥ 2b reperfusion was accomplished with the first pass
Rate of mTICI score 2c reperfusion
The proportion of patients achieving mTICI score ≥ 2c flow
Functional Independence
The proportion of patients achieving Modified Rankin Scale (mRS) ≤2 using the primary treatment modality
Quality of Life Assessment
Measured by Stroke Impact Scale (SIS) Questionnaire
Mortality
All-cause mortality
Intracranial hemorrhage (ICH)
All ICH, as confirmed by imaging
Embolization in new territory (ENT)
Emboli observed immediately after thrombectomy and in a previously unaffected territory
Serious adverse device effects (SADEs)
All SADEs
Serious adverse events
All serious adverse events

Full Information

First Posted
September 27, 2019
Last Updated
October 12, 2023
Sponsor
Imperative Care, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT04129125
Brief Title
The Imperative Trial: Treatment of Acute Ischemic Stroke With the Zoom Reperfusion System
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
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 1, 2021 (Actual)
Primary Completion Date
March 2024 (Anticipated)
Study Completion Date
June 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Imperative Care, Inc.

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

5. Study Description

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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ischemic Stroke, Acute Stroke
Keywords
stroke, thrombectomy, Zoom, aspiration, reperfusion, mRS

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Prospective, multicenter, open-label with independent outcome assessments.
Masking
None (Open Label)
Masking Description
Reperfusion will be graded by an independent core lab that is not an enrolling investigational site. Neurological Outcome Assessors (NIHSS assessment): Neurological outcome assessors who will perform post-procedure 24-hour NIHSS assessments are NIHSS certified team members not performing the thrombectomy procedure and with no financial conflict of interest with Imperative Care, Inc. Functional Outcome Assessors (mRS assessment): Functional outcome assessors who will perform post-procedure assessments are part of achieving unbiased study objectives. They will not have access to patient data.
Allocation
N/A
Enrollment
262 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Zoom Reperfusion System
Arm Type
Experimental
Arm Description
The subject will undergo the endovascular thrombectomy procedure under general anesthesia or conscious sedation. The Imperative Care .088" Catheter will be used to gain access to the vasculature and direct aspiration of the clot will be attempted where feasible. The Zoom Reperfusion System must be the initial and primary device used to remove thrombus.
Intervention Type
Device
Intervention Name(s)
Zoom Reperfusion System
Intervention Description
Thrombectomy
Primary Outcome Measure Information:
Title
Primary Efficacy Endpoint
Description
Rate of reperfusion success, defined as achieving mTICI score ≥ 2b flow with the Zoom Reperfusion System (primary treatment modality) without using additional thrombectomy devices or rescue therapy.
Time Frame
Intraprocedural
Title
Primary Safety Endpoint
Description
Rate of symptomatic intracranial hemorrhage (sICH), as confirmed by imaging
Time Frame
24-hour post-procedure
Secondary Outcome Measure Information:
Title
Time to achieve mTICI score ≥ 2b
Description
The time from groin puncture to mTICI score ≥ 2b flow
Time Frame
Intraprocedural
Title
Rate of mTICI score 3 reperfusion
Description
The proportion of patients achieving mTICI score 3 flow
Time Frame
Intraprocedural
Title
First pass success
Description
The proportion of patients where the mTICI score ≥ 2b reperfusion was accomplished with the first pass
Time Frame
Intraprocedural
Title
Rate of mTICI score 2c reperfusion
Description
The proportion of patients achieving mTICI score ≥ 2c flow
Time Frame
Intraprocedural
Title
Functional Independence
Description
The proportion of patients achieving Modified Rankin Scale (mRS) ≤2 using the primary treatment modality
Time Frame
90 days post-procedure
Title
Quality of Life Assessment
Description
Measured by Stroke Impact Scale (SIS) Questionnaire
Time Frame
90 days post-procedure
Title
Mortality
Description
All-cause mortality
Time Frame
90 days post-procedure
Title
Intracranial hemorrhage (ICH)
Description
All ICH, as confirmed by imaging
Time Frame
24-hour post-procedure
Title
Embolization in new territory (ENT)
Description
Emboli observed immediately after thrombectomy and in a previously unaffected territory
Time Frame
Intraprocedural
Title
Serious adverse device effects (SADEs)
Description
All SADEs
Time Frame
90 days post-procedure
Title
Serious adverse events
Description
All serious adverse events
Time Frame
90 days post-procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18 and older NIHSS >=6 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 Pre-event mRS scale 0-1 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 For strokes in anterior circulation, ASPECTS >=6; For strokes in posterior circulation, pc-ASPECTS >=8 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 If indicated per American Heart Association clinical guidelines, thrombolytic therapy should be administered as soon as possible Consenting requirements met according to local IRB or Ethics Committee Exclusion Criteria: Female known to be pregnant at time of admission Patient has suffered a stroke in the past 3 months Presence of an existing or pre-existing large territory infarction Pre-existing neurological or psychiatric disease that would confound the neurological or functional evaluation, e.g., dementia with prescribed anti-cholinesterase inhibitor Known history of severe contrast allergy or absolute contraindication to iodinated contrast Clinical history, past imaging or clinical judgement suggest that the intracranial occlusion is chronic Life expectancy of less than 6 months prior to stroke onset Clinical symptoms suggestive of bilateral stroke or stroke in multiple territories Subject participating in another clinical trial involving an investigational device or drug Known cancer with metastases Evidence of active systemic infection Any known hemorrhagic or coagulation deficiency Imaging Exclusion Criteria: Evidence of intracranial hemorrhage on CT/MRI CTA or MRA evidence of carotid stenosis requiring treatment for intracranial access Excessive vascular access tortuosity or target vessel size that will likely prevent endovascular access with the Imperative Care 0.088" ID Catheters Intracranial stent implanted in the same vascular territory that would preclude the safe deployment/removal of the thrombectomy devices 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 Significant mass effect with midline shift as confirmed on CT/MRI Evidence of intracranial tumor (except small meningioma defined as ≤ 3cm and asymptomatic) as confirmed on CT/MRI Angiographic evidence of pre-existing arterial injury, e.g., carotid dissection, complete cervical carotid occlusion, or vasculitis
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Pojai Phattanagosai
Phone
1.669.228.3908
Email
pphattanagosai@imperativecare.com
First Name & Middle Initial & Last Name or Official Title & Degree
Didem Aksoy
Phone
1.650.644.8293
Email
daksoy@imperativecare.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Raul G Nogueira, MD
Organizational Affiliation
University of Pittsburgh
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Reade A De Leacy, MD
Organizational Affiliation
Icahn School of Medicine at Mount Sinai
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
William J Mack, MD
Organizational Affiliation
University of Southern California
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Emir Deljkich
Organizational Affiliation
Imperative Care, Inc.
Official's Role
Study Director
Facility Information:
Facility Name
Radiology of Huntsville
City
Huntsville
State/Province
Alabama
ZIP/Postal Code
35801
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Farrar Hickey
Email
Farrar.Hickey@hhsys.org
First Name & Middle Initial & Last Name & Degree
Dana Tomalty, MD
Facility Name
Carondelet Neurological Institute St. Joseph's Hospital
City
Tucson
State/Province
Arizona
ZIP/Postal Code
85711
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lucille Pena
Email
Lucille.Pena@tenethealth.com
First Name & Middle Initial & Last Name & Degree
Alexander Coon, MD
Facility Name
University of Southern California
City
Los Angeles
State/Province
California
ZIP/Postal Code
90033
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sandy Leong
Email
sandyleo@med.usc.edu
First Name & Middle Initial & Last Name & Degree
Matthew Tenser, MD
Facility Name
John Muir Health
City
Walnut Creek
State/Province
California
ZIP/Postal Code
94598
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Melanie Aaron
Email
Melenie.Aaron@johnmuirhealth.com
First Name & Middle Initial & Last Name & Degree
Benjamin Yim, MD
Facility Name
Baptist Health
City
Jacksonville
State/Province
Florida
ZIP/Postal Code
32207
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lanaya Lewis
Email
lanaya.lewis@bmcjax.com
First Name & Middle Initial & Last Name & Degree
Amin Aghaebrahim, MD
Facility Name
University of Miami / Jackson Memorial Hospital
City
Miami
State/Province
Florida
ZIP/Postal Code
33136
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ahmed Abdelsalam, MD
Email
AAA824@miami.edu
First Name & Middle Initial & Last Name & Degree
Robert Starke, MD
Facility Name
Tallahassee Neurological Clinic
City
Tallahassee
State/Province
Florida
ZIP/Postal Code
32308
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shelli Roberts
Email
sroberts@tnc-neuro.com
First Name & Middle Initial & Last Name & Degree
Narlin Beaty, MD
Facility Name
Tampa General Hospital / University of South Florida
City
Tampa
State/Province
Florida
ZIP/Postal Code
33606
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jordan Nickels
Email
nickels1@usf.edu
First Name & Middle Initial & Last Name & Degree
Maxim Mokin, MD
Facility Name
Grady Memorial Hospital / Emory University
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30303
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stephen Duong
Email
stephen.duong@emory.edu
First Name & Middle Initial & Last Name & Degree
Jonathan Grossberg, MD
Facility Name
Ochsner Health
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70121
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
James Milburn, MD
Facility Name
Spectrum Health
City
Grand Rapids
State/Province
Michigan
ZIP/Postal Code
49503
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Justin Singer, MD
Facility Name
Munson Medical Center
City
Traverse City
State/Province
Michigan
ZIP/Postal Code
49684
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
DeAnn Mosher
Email
dmosher@mhc.net
First Name & Middle Initial & Last Name & Degree
David Rosenbaum, MD
Facility Name
Cooper University Health Care
City
Camden
State/Province
New Jersey
ZIP/Postal Code
08103
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lindsey Colman
Email
colman-lindsey@cooperhealth.edu
First Name & Middle Initial & Last Name & Degree
Hamza Shaikh, MD
Facility Name
Montefiore Medical Center
City
Bronx
State/Province
New York
ZIP/Postal Code
10467
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Genesis Liriano
Email
gliriano@montefiore.org
First Name & Middle Initial & Last Name & Degree
Neil Haranhalli, MD
Facility Name
The State University of New York at Buffalo
City
Buffalo
State/Province
New York
ZIP/Postal Code
14203
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jennifer Gay
Email
jgay@ubns.com
First Name & Middle Initial & Last Name & Degree
Kenneth Snyder, MD
Facility Name
Mount Sinai
City
New York
State/Province
New York
ZIP/Postal Code
10029
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sukaina Davdani
Email
Sukaina.davdani@mountsinai.org
First Name & Middle Initial & Last Name & Degree
Emily Fiano
Email
Emily.fiano@mountsinai.org
First Name & Middle Initial & Last Name & Degree
Shahram Majidi, MD
Facility Name
The Ohio State University Medical Center
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43235
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Andrea Hesse
Email
andrea.hesse@osumc.edu
First Name & Middle Initial & Last Name & Degree
Shahid Nimjee, MD, PhD
Facility Name
Oklahoma University
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73104
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sanaa Hameed
Email
Sanaa-Hameed@ouhsc.edu
First Name & Middle Initial & Last Name & Degree
Hakeem Shakir, MD
Facility Name
Lehigh Valley Hospital
City
Allentown
State/Province
Pennsylvania
ZIP/Postal Code
18103
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Matt Karpowicz
Phone
610-402-9543
Email
Matthew.Karpowicz@lvhn.org
First Name & Middle Initial & Last Name & Degree
Darryn Schaff, MD
Facility Name
University of Pennsylvania
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Brett Cucchiara, MD
Facility Name
Prisma Health - Upstate
City
Greenville
State/Province
South Carolina
ZIP/Postal Code
29615
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sean Mcdermott
Email
sean.mcdermott3@prismahealth.org
First Name & Middle Initial & Last Name & Degree
Jordan Kinnitt
Email
jordan.kinnitt@prismahealth.org
First Name & Middle Initial & Last Name & Degree
Jan Vargas, MD
Facility Name
Erlanger Health System: Tennessee Interventional and Imaging Associates
City
Chattanooga
State/Province
Tennessee
ZIP/Postal Code
37403
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Amy Knox
Email
amy@tia-pc.com
First Name & Middle Initial & Last Name & Degree
Harris Hawk, MD
Facility Name
Semmes Murphey Foundation / Methodist University Hospital
City
Memphis
State/Province
Tennessee
ZIP/Postal Code
38120
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jessica Ward
Email
jfward@semmes-murphey.com
First Name & Middle Initial & Last Name & Degree
Amanda Nolte
Email
annolte@semmes-murphey.com
First Name & Middle Initial & Last Name & Degree
Daniel Hoit, MD
Facility Name
Baylor Scott and White Research Institute
City
Dallas
State/Province
Texas
ZIP/Postal Code
75204
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mariana Hurutado
Email
Mariana.Hurutado@BSWHealth.org
First Name & Middle Initial & Last Name & Degree
Kennith Layton, MD
Facility Name
Valley Baptist Medical Center
City
Harlingen
State/Province
Texas
ZIP/Postal Code
78550
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gabriel Rios
Email
gabriel.rios@valleybaptist.net
First Name & Middle Initial & Last Name & Degree
Ameer Hassan, DO, FAHA, FSVIN
Facility Name
The University of Texas Health Science Center at Houston // Memorial Hermann Health System
City
Houston
State/Province
Texas
ZIP/Postal Code
77007
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sergio Salazar Marioni
Email
Sergio.A.SalazarMarioni@uth.tmc.edu
First Name & Middle Initial & Last Name & Degree
Sunil Sheth, MD
Facility Name
University of Texas Health Science Center at San Antonio
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78229
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Justin Mascitelli, MD

12. IPD Sharing Statement

Plan to Share IPD
No

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The Imperative Trial: Treatment of Acute Ischemic Stroke With the Zoom Reperfusion System

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