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Acute and Chronic Protective Effects of Peri-interventional Administration of Levosimendan in ST Elevation Myocardial Infarctions

Primary Purpose

Myocardial Infarction, Outcome

Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Levosimendan
Sponsored by
RWTH Aachen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Myocardial Infarction

Eligibility Criteria

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

Inclusion Criteria:

  • STEMI of the anterior wall < 6 hrs
  • capacity to Consent

Exclusion Criteria:

  • previous myocardial infarction or bypass surgery
  • relevant vitium
  • STEMI of the posterior wall
  • any contraindications to MRI
  • unstable hemodynamics (hypotension, catecholamine therapy, severe arrhythmia), -respiratory failure
  • onset of symptoms more than 6 hours.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Placebo Comparator

    Active Comparator

    Active Comparator

    Arm Label

    Placebo

    Bolus Levosimendan

    Bolus and infusion Levosimendan

    Arm Description

    Placebo is given as a Bolus (instead of Bolus application of Levosimendan) over 10 min i.v., starting 10 min before recanalization.

    Levosimendan is given as Bolus (12 µg/kg over 10 min i.v.), starting 10 min before recanalization.

    Levosimendan is given as Bolus (12 µg/kg over 10 min i.v.), starting 10 min before recanalization and additionally as continuous infusion (0.1-0.2 µg/kg/min i. v. for 24 hours).

    Outcomes

    Primary Outcome Measures

    Reduction of the increase in left ventricular end-diastolic volume index (LVEDVi)
    echocardiography and MRI examinations (LVEDVi) and comparison between baseline and 12 months data

    Secondary Outcome Measures

    Size of the acute myocardial damage due to the infarction
    MRI examination (infarction area) and comparison between baseline and 12 months data
    Event-free survival
    collection of data from the patient after 12 months about adverse events as myocardial infarction, stroke, revascularization and death
    functional changes (imaging)
    echocardiography and MRI examinations about LV function
    structural changes
    MRI examinations about fibrosis
    functional changes (spirometry)
    changes of capacity by spirometry.

    Full Information

    First Posted
    January 6, 2017
    Last Updated
    October 25, 2022
    Sponsor
    RWTH Aachen University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03022877
    Brief Title
    Acute and Chronic Protective Effects of Peri-interventional Administration of Levosimendan in ST Elevation Myocardial Infarctions
    Official Title
    Acute and Chronic Protective Effects of Peri-interventional Administration of Levosimendan in ST Elevation Myocardial Infarctions
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2022
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    Rationale obsolete
    Study Start Date
    June 2017 (Anticipated)
    Primary Completion Date
    December 2018 (Anticipated)
    Study Completion Date
    December 2018 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    RWTH Aachen University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    In the proposed project the investigators want to assess whether the approach of the post-conditioning by Levosimendan in patients with acute STEMI is safe and reproducible, can be used with a positive influence on the outcomes with respect to myocardial damage, cardiac left ventricular remodeling, myocardial function, the occurrence of cardiac events and quality of life.
    Detailed Description
    An acute ST-elevation myocardial infarction (STEMI) is a severe disease that triggers an adverse remodeling, and served in progressive heart failure with a case fatality rate of 50% in 5 years. The opening of the occluded vessel is the first and most important therapy, the reperfusion improved both the function as well as the long-term survival. At the same time, experimental and clinical studies show, however, that this reperfusion self-reinforced damage of the myocardium. An additional Intervention in this trigger phase could not only reduce the acute damage, but long-term protective effects. Both effects could be an approach for the Calcium-Sensitizer Levosimendan in the animal model. So far, no clear effect on the remodeling and survive was demonstrated after myocardial infarction in the clinic. This could be mainly due to the delayed application in relation to the reperfusion and on the selection of suitable methods for the presentation of the effects on myocardial structure and function. In the proposed project the investigators want to assess whether the approach of the post-conditioning by Levosimendan in patients with acute STEMI is safe and reproducible, can be used with a positive influence on the outcomes with respect to myocardial damage, cardiac left ventricular remodeling, myocardial function, the occurrence of cardiac events and quality of life.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Myocardial Infarction, Outcome

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Participant
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Placebo
    Arm Type
    Placebo Comparator
    Arm Description
    Placebo is given as a Bolus (instead of Bolus application of Levosimendan) over 10 min i.v., starting 10 min before recanalization.
    Arm Title
    Bolus Levosimendan
    Arm Type
    Active Comparator
    Arm Description
    Levosimendan is given as Bolus (12 µg/kg over 10 min i.v.), starting 10 min before recanalization.
    Arm Title
    Bolus and infusion Levosimendan
    Arm Type
    Active Comparator
    Arm Description
    Levosimendan is given as Bolus (12 µg/kg over 10 min i.v.), starting 10 min before recanalization and additionally as continuous infusion (0.1-0.2 µg/kg/min i. v. for 24 hours).
    Intervention Type
    Drug
    Intervention Name(s)
    Levosimendan
    Intervention Description
    In a prospective randomized setting, patients are included with an acute STEMI of the anterior wall. A bolus administration Levosimendan with/without following continuous infusion over 24 hours compared to a control group (placebo) will be examined. The initiation of therapy is carried out for 10 min. prior to reperfusion. The coronary Intervention is performed immediately after inclusion at the latest within 6 hours after the onset of symptoms. The administration of Levosimendan is based on a fixed schema: Bolus: 12 µg/kg over 10 min I. V., starting 10 min before recanalization and an addition of 0.1-0.2 µg/kg/min i. v. for 24 hours in the continuous infusion group.
    Primary Outcome Measure Information:
    Title
    Reduction of the increase in left ventricular end-diastolic volume index (LVEDVi)
    Description
    echocardiography and MRI examinations (LVEDVi) and comparison between baseline and 12 months data
    Time Frame
    12 months after coronary intervention due to the infarction
    Secondary Outcome Measure Information:
    Title
    Size of the acute myocardial damage due to the infarction
    Description
    MRI examination (infarction area) and comparison between baseline and 12 months data
    Time Frame
    12 months after coronary intervention due to the infarction
    Title
    Event-free survival
    Description
    collection of data from the patient after 12 months about adverse events as myocardial infarction, stroke, revascularization and death
    Time Frame
    12 months after coronary intervention due to the infarction
    Title
    functional changes (imaging)
    Description
    echocardiography and MRI examinations about LV function
    Time Frame
    12 months after coronary intervention due to the infarction
    Title
    structural changes
    Description
    MRI examinations about fibrosis
    Time Frame
    12 months after coronary intervention due to the infarction
    Title
    functional changes (spirometry)
    Description
    changes of capacity by spirometry.
    Time Frame
    12 months after coronary intervention due to the infarction

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: STEMI of the anterior wall < 6 hrs capacity to Consent Exclusion Criteria: previous myocardial infarction or bypass surgery relevant vitium STEMI of the posterior wall any contraindications to MRI unstable hemodynamics (hypotension, catecholamine therapy, severe arrhythmia), -respiratory failure onset of symptoms more than 6 hours.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Michael Becker
    Organizational Affiliation
    Cardiology, RWTH University Hospital Aachen
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    26965540
    Citation
    Brooks GC, Lee BK, Rao R, Lin F, Morin DP, Zweibel SL, Buxton AE, Pletcher MJ, Vittinghoff E, Olgin JE; PREDICTS Investigators. Predicting Persistent Left Ventricular Dysfunction Following Myocardial Infarction: The PREDICTS Study. J Am Coll Cardiol. 2016 Mar 15;67(10):1186-1196. doi: 10.1016/j.jacc.2015.12.042.
    Results Reference
    background
    PubMed Identifier
    11748117
    Citation
    Kloner RA, Jennings RB. Consequences of brief ischemia: stunning, preconditioning, and their clinical implications: part 2. Circulation. 2001 Dec 18;104(25):3158-67. doi: 10.1161/hc5001.100039.
    Results Reference
    result
    PubMed Identifier
    17855673
    Citation
    Yellon DM, Hausenloy DJ. Myocardial reperfusion injury. N Engl J Med. 2007 Sep 13;357(11):1121-35. doi: 10.1056/NEJMra071667. No abstract available.
    Results Reference
    result
    PubMed Identifier
    18359896
    Citation
    du Toit EF, Smith W, Muller C, Strijdom H, Stouthammer B, Woodiwiss AJ, Norton GR, Lochner A. Myocardial susceptibility to ischemic-reperfusion injury in a prediabetic model of dietary-induced obesity. Am J Physiol Heart Circ Physiol. 2008 May;294(5):H2336-43. doi: 10.1152/ajpheart.00481.2007. Epub 2008 Mar 21.
    Results Reference
    result
    PubMed Identifier
    19426242
    Citation
    Hein M, Roehl AB, Baumert JH, Scherer K, Steendijk P, Rossaint R. Anti-ischemic effects of inotropic agents in experimental right ventricular infarction. Acta Anaesthesiol Scand. 2009 Aug;53(7):941-8. doi: 10.1111/j.1399-6576.2009.01994.x. Epub 2009 May 6.
    Results Reference
    result
    PubMed Identifier
    15023554
    Citation
    Kin H, Zhao ZQ, Sun HY, Wang NP, Corvera JS, Halkos ME, Kerendi F, Guyton RA, Vinten-Johansen J. Postconditioning attenuates myocardial ischemia-reperfusion injury by inhibiting events in the early minutes of reperfusion. Cardiovasc Res. 2004 Apr 1;62(1):74-85. doi: 10.1016/j.cardiores.2004.01.006.
    Results Reference
    result
    PubMed Identifier
    23063476
    Citation
    Qarawani D, Cohen A, Nahir M, Hasin Y. Facilitation of left ventricular function recovery post percutaneous coronary intervention by levosimendan. Int J Cardiol. 2013 Sep 20;168(1):237-42. doi: 10.1016/j.ijcard.2012.09.088. Epub 2012 Oct 11.
    Results Reference
    result

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    Acute and Chronic Protective Effects of Peri-interventional Administration of Levosimendan in ST Elevation Myocardial Infarctions

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