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Withdrawn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
About this trial
This is an interventional treatment trial for Myocardial Infarction
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.
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
NCT ID
NCT03022877
First Posted
January 6, 2017
Last Updated
October 25, 2022
Sponsor
RWTH Aachen University
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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