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Utilization of Diagnostic Ultrasound in the Detection and Therapy of Acute Coronary Syndromes

Primary Purpose

Acute Coronary Syndrome, Myocardial Infarction

Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Use of intermittent high MI impulses during echocardiogram
Sponsored by
University of Nebraska
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Coronary Syndrome focused on measuring ST elevated myocardial infarction, Acute coronary syndrome, MRX 801, Echocardiography

Eligibility Criteria

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

Inclusion Criteria:

  1. Male or female, age ≥ 30 years.
  2. Chest Pain occurring lasting less than six hours from onset, and EKG evidence of an acute ST segment elevation myocardial infarction.
  3. Arrival in the Emergency Department with above inclusion criteria between 7 am and 7pm.

Exclusion Criteria:

  1. Known or suspected hypersensitivity to ultrasound contrast agent used for the study.
  2. Complicated hemodynamic instability (i.e., NYHA Class IV heart failure, unstable angina at rest despite medical therapy).
  3. Life expectancy of less than two months or terminally ill.
  4. Heart transplant recipient, hypertrophic cardiomyopathy, severe valvular disease, acute myo- or pericarditis.
  5. Contraindication to Heart Catheterization
  6. Known bleeding diathesis or contraindication to glycoprotein 2b/3a inhibitors or aspirin.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    High MI impulses, myocardial infarction, echocardiography

    Arm Description

    Using the transthoracic three dimensional imaging probe, low mechanical index (MI) will examine wall motion. Intermittent high MI impulses will be administered over the microvasculature where there are wall motion abnormalities using an imaging plan that best aligns itself with the risk area. One vial of MRX 801 to be infused intravenously during echocardiography with high mechanical index impulses.

    Outcomes

    Primary Outcome Measures

    Improved microvascular recanalization and epicardial recanalization rates in STEMI as assessed by coronary angiography and recovery of regional microvascular perfusion and function in the post-infarction period.
    Improved microvascular recanalization and epicardial recanalization rates in STEMI as assessed by coronary angiography and recovery of regional microvascular perfusion and function in the post-infarction period.

    Secondary Outcome Measures

    Full Information

    First Posted
    August 5, 2009
    Last Updated
    August 10, 2023
    Sponsor
    University of Nebraska
    Collaborators
    Microvascular Therapeutics, LLC, The Ruth and Bruce Rappaport Faculty of Medicine, Amsterdam University Medical Centers (UMC), Location Academic Medical Center (AMC), InCor Heart Institute, Bnai Zion Medical Center
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00955136
    Brief Title
    Utilization of Diagnostic Ultrasound in the Detection and Therapy of Acute Coronary Syndromes
    Official Title
    Utilization of Diagnostic Ultrasound in the Detection and Therapy of Acute Coronary Syndromes
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2023
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    The study was withdrawn due to many implementation difficulties.
    Study Start Date
    July 2009 (Anticipated)
    Primary Completion Date
    January 25, 2010 (Actual)
    Study Completion Date
    January 25, 2010 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University of Nebraska
    Collaborators
    Microvascular Therapeutics, LLC, The Ruth and Bruce Rappaport Faculty of Medicine, Amsterdam University Medical Centers (UMC), Location Academic Medical Center (AMC), InCor Heart Institute, Bnai Zion Medical Center

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The study will see if mechanical impulses delivered by an echocardiographic probe during a continuous infusion of MRX 801 are capable of improving blood flow in smaller heart vessels in patients with acute coronary syndromes.
    Detailed Description
    Pre-clinical studies have indicated that, during a continuous infusion of intravenous perfluorocarbon-containing microbubbles, the ultrasonic power delivered from a diagnostic ultrasound transducer is capable of restoring microcirculatory flow and improving epicardial recanalization rates following acute coronary thrombotic occlusions. Since both diagnostic ultrasound and intravenous infusions of microbubbles are a Class I indication to assess regional and global left ventricular function and risk area in patients with ST segment elevation myocardial infarction (STEMI), this pilot study will examine whether diagnostic assessments of left ventricular function and risk area size impacts epicardial recanalization rates and infarct size in STEMI. The aim of this study is to test whether guided high mechanical index impulses from a diagnostic transducer during a continuous infusion of intravenous microbubbles are capable of improving microvascular recanalization and epicardial recanalization rates in STEMI, as assessed by coronary angiography, and recovery of regional microvascular perfusion and function in the post-infarction period.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Acute Coronary Syndrome, Myocardial Infarction
    Keywords
    ST elevated myocardial infarction, Acute coronary syndrome, MRX 801, Echocardiography

    7. Study Design

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

    8. Arms, Groups, and Interventions

    Arm Title
    High MI impulses, myocardial infarction, echocardiography
    Arm Type
    Experimental
    Arm Description
    Using the transthoracic three dimensional imaging probe, low mechanical index (MI) will examine wall motion. Intermittent high MI impulses will be administered over the microvasculature where there are wall motion abnormalities using an imaging plan that best aligns itself with the risk area. One vial of MRX 801 to be infused intravenously during echocardiography with high mechanical index impulses.
    Intervention Type
    Device
    Intervention Name(s)
    Use of intermittent high MI impulses during echocardiogram
    Intervention Description
    Using the transthoracic three dimensional imaging probe, low mechanical index (MI) will examine wall motion. Intermittent high MI impulses will be administered over the microvasculature where there are wall motion abnormalities using an imaging plan that best aligns itself with the risk area. One vial of MRX 801 to be infused intravenously during echocardiography with high mechanical index impulses.
    Primary Outcome Measure Information:
    Title
    Improved microvascular recanalization and epicardial recanalization rates in STEMI as assessed by coronary angiography and recovery of regional microvascular perfusion and function in the post-infarction period.
    Description
    Improved microvascular recanalization and epicardial recanalization rates in STEMI as assessed by coronary angiography and recovery of regional microvascular perfusion and function in the post-infarction period.
    Time Frame
    6 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    30 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Male or female, age ≥ 30 years. Chest Pain occurring lasting less than six hours from onset, and EKG evidence of an acute ST segment elevation myocardial infarction. Arrival in the Emergency Department with above inclusion criteria between 7 am and 7pm. Exclusion Criteria: Known or suspected hypersensitivity to ultrasound contrast agent used for the study. Complicated hemodynamic instability (i.e., NYHA Class IV heart failure, unstable angina at rest despite medical therapy). Life expectancy of less than two months or terminally ill. Heart transplant recipient, hypertrophic cardiomyopathy, severe valvular disease, acute myo- or pericarditis. Contraindication to Heart Catheterization Known bleeding diathesis or contraindication to glycoprotein 2b/3a inhibitors or aspirin.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Thomas R Porter, MD
    Organizational Affiliation
    University of Nebraska
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Utilization of Diagnostic Ultrasound in the Detection and Therapy of Acute Coronary Syndromes

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