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Trial record 1 of 1 for:    NCT04201132
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Protection Against Emboli During Carotid Artery Stenting Using the Neuroguard IEP System (PERFORMANCEII)

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ClinicalTrials.gov Identifier: NCT04201132
Recruitment Status : Active, not recruiting
First Posted : December 17, 2019
Last Update Posted : April 4, 2023
Sponsor:
Information provided by (Responsible Party):
Contego Medical, Inc.

Brief Summary:
A prospective, multicenter single-arm, open label study to evaluate the safety and effectiveness of the Neuroguard IEP System for the treatment of carotid artery stenosis in subjects at elevated risk for adverse events following carotid endarterectomy (CEA). The Neuroguard IEP System is a 3-in-1 carotid stent delivery system consisting of an angioplasty balloon, an integrated embolic protection device and a nitinol self-expanding stent loaded over the balloon and constrained by an outer sheath. Eligible patients between 20 and 80 years of age have been diagnosed with either de-novo atherosclerotic or post CEA restenotic lesion(s) in the internal carotid arteries (ICA) or at the carotid bifurcation with ≥50% stenosis if symptomatic or ≥80% stenosis if asymptomatic (both defined by angiography using NASCET methodology). Symptomatic patients are defined as having stroke or TIA ipsilateral to the carotid lesion within 180 days of the procedure within the hemisphere supplied by the target vessel. Enrolled subjects will be followed at 30 days, 6 months, 12 months, 24 months and 36 months.

Condition or disease Intervention/treatment Phase
Carotid Artery Stenosis Carotid Artery Diseases Carotid Stenosis Device: Carotid artery stenting with Neuroguard IEP System Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 305 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Protection Against Emboli During Carotid Artery Stenting Using a 3-in-1 Delivery System Comprised of a Post-dilation Balloon, Integrated Embolic Filter and a Novel Carotid Stent II
Actual Study Start Date : June 12, 2020
Actual Primary Completion Date : November 10, 2022
Estimated Study Completion Date : September 2025

Arm Intervention/treatment
Experimental: Carotid artery stenting
Carotid artery stenting procedure with Neuroguard IEP System
Device: Carotid artery stenting with Neuroguard IEP System
Carotid artery stenting (treatment) with the Neuroguard IEP 3-in-1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection




Primary Outcome Measures :
  1. Rate of stroke, death and myocardial infarction (MI) [ Time Frame: 30 days ]
  2. Rate of ipsilateral stroke [ Time Frame: 12 months ]

Secondary Outcome Measures :
  1. Technical success [ Time Frame: Day of procedure ]
    Successful stent deployment, successful filter deployment and retrieval, successful stent post-dilation and successful delivery system retrieval

  2. Procedure success [ Time Frame: Day of procedure ]
    Successful stent implantation with <50% residual stenosis

  3. Target lesion revascularization (TLR) [ Time Frame: 12 months ]
  4. In-stent restenosis (ISR) [ Time Frame: 12 months, 24 months, 36 months ]
  5. Major stroke [ Time Frame: 30 days ]
  6. Minor stroke [ Time Frame: 30 days ]
  7. Transient ischemic attack (TIA) [ Time Frame: 30 days ]
  8. Neurological death [ Time Frame: 12 months ]


Information from the National Library of Medicine

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Ages Eligible for Study:   20 Years to 80 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

General Inclusion Criteria

  1. Male and non-pregnant, non-breastfeeding female subjects whose age is ≥ 20 years and ≤ 80.
  2. Patient is willing and capable of complying with all study protocol requirements, including the specified follow-up visits and can be contacted by telephone.
  3. Patient or his/her authorized legal representative must sign a written informed consent form that has been approved by the local governing Institutional Review Board (IRB)/ Ethics Committee (EC) of the respective clinical site.
  4. Patient is diagnosed with carotid artery stenosis treatable with carotid artery stenting and is considered a high operative risk for CEA.
  5. Patient is diagnosed with either:

    1. Symptomatic carotid stenosis ≥ 50% as determined by angiography using NASCET methodology. Symptomatic is defined as ipsilateral transient monocular blindness: amaurosis fugax; ipsilateral carotid transient ischemic attack (TIA), with neurologic symptoms persisting less than 24 hours; or ipsilateral non-disabling stroke within 180 days of the procedure; or
    2. Asymptomatic carotid stenosis ≥ 80% as determined by angiography using NASCET methodology.
  6. Patient has a modified Rankin Scale score of ≤ 2 at the time of informed consent.
  7. Females of child-bearing potential have a negative pregnancy test within 24 hours of the index procedure.
  8. Patient is willing and able to take dual antiplatelet therapy for a minimum of 30 days following the index procedure.

Angiographic Inclusion Criteria

  1. Target lesion located at the carotid bifurcation and/or proximal internal carotid artery (ICA).
  2. Single de novo or restenotic (post carotid endarterectomy (CEA)) target lesion or severe tandem lesions that can be covered by a single Neuroguard stent.
  3. Target lesion length is ≤ 20 mm (for 30 mm stents) or is ≤ 30 mm (for 40 mm stents).
  4. Index vessel diameter (segment covered by the mid-portion of the stent) between 4.0 mm and 6.0 mm at the site of the target lesion.
  5. Distal vessel diameter at the site of filter deployment is between 4.0 mm to 7.0 mm.
  6. Distal common carotid artery diameter (segment covered by proximal portion of the stent) is between 4.0 mm and 8.0 mm
  7. Sufficient landing zone exists in the cervical internal carotid artery distal to the target lesion to allow for the safe and successful deployment of both the primary embolic protection filter and the Neuroguard filter.

High Risk for CEA Conditions For inclusion in the study, a patient must meet at least one significant anatomic or comorbid high risk conditions listed below. Patients at high risk for CEA are defined as having significant comorbidities and/or anatomic risk factors and would be poor candidates for carotid endarterectomy (CEA) in the opinion of a physician.

High Anatomic Risk for CEA Conditions

  1. Target lesion at or above C2 (level of jaw) or below the clavicle.
  2. Inability to extend the head due to cervical arthritis or other cervical disorders.
  3. History of radiation treatment to the neck or radical neck dissection
  4. Prior head and neck surgery in the region of the carotid artery.
  5. Spinal immobility of the neck.
  6. Tracheostomy or tracheostoma.
  7. Hostile neck or surgically inaccessible lesion
  8. Laryngeal palsy or laryngectomy.
  9. Severe tandem lesions (total length must be ≤ 30 mm and must be covered with one stent).
  10. Occlusion of the contralateral CCA or ICA.
  11. Severe bilateral ICA stenosis.

High Co-morbid Risk Conditions for CEA

  1. Patient is ≥ 70 years of age (maximum 80 years) at the time of enrollment.
  2. NYHA Class III or IV congestive heart failure (CHF)
  3. Chronic obstructive pulmonary disease (COPD) with FEV1 < 50 or on intermittent or chronic oxygen therapy.
  4. Left ventricular ejection fraction (LVEF) ≤ 35%
  5. Unstable angina
  6. History of recent MI (between 14 days and 6 weeks prior to index the procedure)
  7. Coronary artery disease with two or more vessels with ≥ 70% stenosis
  8. Planned coronary artery bypass grafting (CABG) or valve replacement surgery between 31 and 60 days after CAS procedure
  9. Peripheral vascular surgery or abdominal aortic aneurysm repair is required and planned between 31 and 60 days following CAS procedure
  10. Contralateral laryngeal nerve paralysis
  11. Restenosis following a prior carotid endarterectomy (CEA).

General Exclusion Criteria:

  1. Life expectancy of less than one year, cancer with metastatic spread, undergoing active chemotherapy treatment, or currently requiring an organ transplantation.
  2. An evolving acute stroke.
  3. Anticipated or potential sources of emboli including left ventricular aneurysm, severe cardiomyopathy, aortic or mitral mechanical heart valve, severe calcific aortic stenosis (valve area < 1.0 cm2), endocarditis, moderate to severe mitral stenosis, known previously symptomatic PFO, left atrial thrombus, any intracardiac mass or DVT or PE treated within the past 12 months.
  4. History of paroxysmal atrial flutter or atrial fibrillation requiring chronic anticoagulation
  5. History of chronic atrial flutter or atrial fibrillation.
  6. Anticoagulation with Phenprocoumon (Marcumar®), warfarin, or a direct thrombin inhibitor, or anti-Xa agents within 14 days of the index procedure.
  7. Acute febrile illness (temperature > 100.4F or 38C) or active infection.
  8. Subjects with presumptive or confirmed SARS-CoV-2/COVID-19 infection.

    • A SARS-CoV-2/COVID-19 test shall be performed 72 hours prior to the index procedure for all subjects
    • Note: If a subject has confirmed SARS-CoV-2/COVID-19 infection (SARSCoV-2/COVID-19+), eligibility may be re-established 21 days following diagnosis if infection is asymptomatic and 21 days following resolution of symptoms if infection is symptomatic.
  9. Acute myocardial infarction < 14 days prior to index procedure.
  10. Any major surgical procedure (i.e. intraabdominal or intrathoracic surgery or any surgery / interventional procedure involving cardiac or vascular system) 30 days prior to or following the index procedure.
  11. History of major disabling stroke with substantial residual disability (modified Rankin score ≥ 3)
  12. Known severe carotid stenosis or complete occlusion contralateral to the target lesion requiring treatment within 30 days of the index procedure.
  13. Other neurological deficit not due to stroke that may confound the neurological assessments.
  14. Dementia considered other than mild.
  15. Known hypersensitivity to nitinol or its components (e.g. nickel, titanium).
  16. History of intracranial hemorrhage within 90 days prior to the index procedure.
  17. History of GI bleed within 30 days prior to the index procedure
  18. Chronic renal insufficiency (serum creatinine ≥ 2.5 ml/dL or estimated GFR < 30 cc/min)
  19. Any condition that precludes proper angiographic assessment or makes percutaneous arterial access unsafe (e.g., severe hepatic impairment, malignant hypertension, morbid obesity).
  20. Known hypersensitivity to contrast media that cannot be adequately premedicated.
  21. Hemoglobin (Hgb) < 8 gm/dL, platelet count < 100,000, INR > 1.5 (irreversible), or heparin-induced thrombocytopenia.
  22. History or current indication of bleeding diathesis or coagulopathy including thrombocytopenia or an inability to receive heparin in amounts sufficient to maintain an activated clot time at ≥ 250 seconds.
  23. Contraindication to standard of care study medications, including antiplatelet therapy or aspirin.
  24. Currently enrolled in another interventional device or drug study that has not yet reached the primary endpoint.
  25. Potential for subject non-compliance with protocol-required follow up or anti platelet medication in the opinion of the investigator.

Angiographic Exclusion Criteria

  1. Total occlusion of the target carotid artery.
  2. Previously placed stent in the ipsilateral carotid artery.
  3. Severe calcification or vascular tortuosity of the target vessel that may preclude the safe introduction of the sheath, guiding catheter, distal filter, Neuroguard stent or Neuroguard filter. Excessive circumferential calcification of the target lesion is defined as >3 mm of thickness of calcification seen in orthogonal views on fluoroscopy. Severe vascular tortuosity is defined as 2 or more bends of 90 degrees or more within 4 cm of the target lesion.
  4. Qualitative characteristics of stenosis and stenosis-length of carotid bifurcation (common carotid) and/or ipsilateral external carotid artery, that preclude the safe introduction of the sheath.
  5. Angulation or tortuosity (≥ 90 degree) of the innominate and common carotid artery (CCA) that precludes safe, expeditious sheath placement or that will transmit a severe loop to the internal carotid after sheath placement.
  6. Angiographic evidence of a mobile filling defect or fresh thrombus in the target carotid artery.
  7. Presence of "string sign" of the target lesion (a sub-totally occluded, long segment of the true lumen of the artery with markedly reduced contrast flow).
  8. Non-atherosclerotic carotid stenosis (e.g. dissection, fibromuscular dysplasia)
  9. Proximal/ostial CCA, innominate stenosis, or intracranial stenosis located distal to the target stenosis that is more severe that target stenosis.
  10. Patient in whom percutaneous vascular access is not possible, including severe tortuosity or stenosis that requires additional endovascular procedures to facilitate aortic arch access or that prevents safe and expeditious access.
  11. Patient with intracranial pathology that, in the opinion of the investigator, makes the patient inappropriate for study participation (e.g., arteriovenous malformations, brain tumor, microangiopathy or large vessel cerebral vascular disease, etc) or that would confound the neurological evaluation.
  12. Known mobile plaque or thrombus in the aortic arch.
  13. Type III aortic arch.
  14. Angiographic, CT, MR or ultrasound evidence of severe atherosclerosis, tortuosity or angulation of the aortic arch or origin of the innominate or common carotid arteries that would preclude or make difficult safe passage of the sheath and other endovascular devices to the target artery as needed for carotid stenting.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04201132


Locations
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United States, Iowa
University of Iowa Hospital and Clinics
Iowa City, Iowa, United States, 52242
United States, New York
University at Buffalo Neurosurgery
Buffalo, New York, United States, 14203
St. Francis Hospital
Roslyn, New York, United States, 11576
United States, North Carolina
North Carolina Heart and Vascular Research
Raleigh, North Carolina, United States, 27607
United States, Pennsylvania
St. Vincent Hospital
Erie, Pennsylvania, United States, 16502
Pinnacle Health Cardiovascular Institute
Harrisburg, Pennsylvania, United States, 17043
United States, South Dakota
North Central Heart Institute
Sioux Falls, South Dakota, United States, 57108
United States, Tennessee
Ballad Wellmont Holston Valley Medical Center
Kingsport, Tennessee, United States, 37660
Germany
Sankt Gertrauden-Krankenhaus GmbH
Berlin, Germany, 10713
Cardiovascular Centre Frankfurt
Frankfurt, Germany
Medizinisches Versorgungszentrum Prof. Mathey, Prof. Schofer GmbH
Hamburg, Germany
Universitätsklinikum Leipzig
Leipzig, Germany, 04103
Sponsors and Collaborators
Contego Medical, Inc.
Investigators
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Principal Investigator: William A Gray, MD Main Line Health
Principal Investigator: Ralf Langhoff, MD Sankt Gertrauden Krankenhaus
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Responsible Party: Contego Medical, Inc.
ClinicalTrials.gov Identifier: NCT04201132    
Other Study ID Numbers: CSP1400
First Posted: December 17, 2019    Key Record Dates
Last Update Posted: April 4, 2023
Last Verified: March 2023
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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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
Product Manufactured in and Exported from the U.S.: Yes
Additional relevant MeSH terms:
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Carotid Stenosis
Carotid Artery Diseases
Constriction, Pathologic
Pathological Conditions, Anatomical
Cerebrovascular Disorders
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Arterial Occlusive Diseases
Vascular Diseases
Cardiovascular Diseases