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Ticagrelor and Intracoronary Morphine in Patients Undergoing Primary Percutaneous Coronary Intervention

Primary Purpose

ST-Segment Elevation Myocardial Infarction

Status
Unknown status
Phase
Phase 2
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Ticagrelor
Clopidogrel
Morphine Sulfate
Saline
Sponsored by
Hyeon-Cheol Gwon
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for ST-Segment Elevation Myocardial Infarction

Eligibility Criteria

20 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers
  1. Inclusion criteria

    • Subject must be at least 20 years of age.
    • Patients undergoing primary PCI for STEMI

      • Diagnosis of STEMI: ST-segment elevation >0.1 millivolt in ≥2 contiguous leads or (presumably) new left bundle branch block
      • Presence of symptoms less than 12 hours
    • Additional inclusion criteria for intracoronary morphine

      • TIMI flow grade 0 or 1 of infarct related arteries
  2. Exclusion Criteria:

    • Known hypersensitivity or contraindication to study medications or contrast
    • Female of childbearing potential, unless a recent pregnancy test is negative, who possibly plan to become pregnant any time after enrollment into this study.
    • Rescue PCI after thrombolysis or facilitated PCI
    • Cardiogenic shock or cardiopulmonary resuscitation before randomization
    • Known chronic hepatic disease
    • Known renal dysfunction (creatinine level 3.0mg/dL or dependence on dialysis).
    • Decompensated chronic obstructive pulmonary disease or active asthma at inclusion
    • Mechanical ventilation at inclusion
    • Brain injury or intracranial hypertension
    • Acute alcohol intoxication
    • Known ulcerative colitis
    • Active epilepsy
    • Contraindications to undergo MRI imaging include any of the following

      • A cardiac pacemaker or implantable defibrillator; any implanted or magnetically activated device; or any history indicating contraindication to MRI including claustrophobia or allergy to gadolinium
    • Current use of oral anticoagulant
    • An increased risk of bradycardia

      • Sinus node dysfunction, atrioventricular dysfunction, or heart rate <40/min
    • Patients receiving clopidogrel 300 mg or more before randomization
    • One of followings

      • history of intracranial bleeding
      • intracranial tumor, arteriovenous malformation or aneurysm
      • stroke within past 3 months
    • Active bleeding of internal organ or bleeding diathesis
    • Acute aortic dissection

Sites / Locations

  • Samsung Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Active Comparator

Arm Label

Ticagrelor + Intracoronary Morphine

Ticagrelor + Intracoronary Saline

Clopidogrel + Intracoronary Morphine

Clopidogrel + Intracoronary Saline

Arm Description

180 mg loading pre-PCI followed by 90 mg bid for 5 days. Intracoronary Morphine Sulfate 3 mg + Saline 3 ml mix.

180 mg loading pre-PCI followed by 90 mg bid for 5 days. Saline 3 ml intracoronary injection.

600 mg loading pre-PCI followed by 75 mg qd for 5 days. Morphine Sulfate 3 mg + Saline 3 ml mix intracoronary injection.

600 mg loading pre-PCI followed by 75 mg qd for 5 days. Saline 3 ml intracoronary injection.

Outcomes

Primary Outcome Measures

Myocardial infarct size measured by magnetic resonance imaging (MRI) at 3-5 days after the index procedure

Secondary Outcome Measures

Rate of complete ST-segment resolution on ECG obtained 30 minutes after the procedure
Enzymatic Infarct size by creatine kinase-MB (area under curve)
Myocardial salvage index measured by MRI
Major adverse cardiac events (a composite of death, myocardial infarction, severe heart failure, or stent thrombosis)
The extent of microvascular obstruction measured by MRI
The number of segments with >75% of infarct transmurality measured by MRI
The presence of myocardial hemorrhage measured by MRI

Full Information

First Posted
November 23, 2012
Last Updated
July 4, 2016
Sponsor
Hyeon-Cheol Gwon
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1. Study Identification

Unique Protocol Identification Number
NCT01738100
Brief Title
Ticagrelor and Intracoronary Morphine in Patients Undergoing Primary Percutaneous Coronary Intervention
Official Title
Effects of Ticagrelor and Intracoronary Morphine on Myocardial Salvage in Patients With ST-Segment Elevation Myocardial Infarction Undergoing Primary Percutaneous Coronary Intervention
Study Type
Interventional

2. Study Status

Record Verification Date
October 2014
Overall Recruitment Status
Unknown status
Study Start Date
September 2012 (undefined)
Primary Completion Date
December 2016 (Anticipated)
Study Completion Date
December 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Hyeon-Cheol Gwon

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
A 2 by 2 factorial, multicenter, prospective, randomized, open-label, blinded endpoint trial. Patients undergoing primary PCI for STEMI will be eligible. Enrolled patients will be randomly assigned to the ticagrelor group or the clopidogrel group in a 1:1 ratio. After emergent coronary angiography, patients who have thrombolysis in myocardial infarction (TIMI) flow grade <2 in coronary angiogram will be randomized again, to either bolus intracoronary injection of morphine sulfate or saline in a 1:1 ratio. Randomization will be stratified by infarct location (anterior vs. non-anterior), and morphine use for pain control before study enroll (for only intracoronary morphine).
Detailed Description
1.1. Ticagrelor versus Clopidogrel In spite of timely and successful reperfusion with primary percutaneous coronary intervention (PCI), the mortality rate still remains high1 and substantial numbers of patients suffer from subsequent left ventricular dysfunction or heart failure after ST-segment elevation myocardial infarction (STEMI). One of limitations of primary PCI is distal embolization and effective antiplatelet therapy is needed in patients with STEMI. Clopidogrel is a representative P2Y12 receptor antagonist and has shown consistent efficacy in patients with acute coronary syndromes. However, clopidogrel is a prodrug and has to be converted to an active metabolite to inhibit P2Y12 receptor. Therefore, onset of effect is relatively slow, antiplatelet effect is moderate, and response to clopidogrel shows wide individual variability. Ticagrelor is a new, direct, reversible P2Y12 receptor antagonist, which has rapid and potent antiplatelet effect. In patients who have an acute coronary syndrome with or without ST-segment elevation, treatment with ticagrelor as compared with clopidogrel significantly reduced the rate of death from vascular causes, myocardial infarction, or stroke without an increase in the rate of overall major bleeding. However, there has been no data whether ticagrelor can reduce infarct size compared with clopidogrel in patients undergoing primary PCI. 1.2. Intracoronary morphine administration Lethal reperfusion injury accounts for up to 50% of the final size of a myocardial infarct.5,6 Therefore, adjunctive therapy that is effective in preventing lethal reperfusion injury is needed to potentiate the benefits of primary PCI. During the past few decades, a large number of animal studies demonstrated that commonly used opioids could provide cardioprotection against ischemia-reperfusion injury. Opioid-induced preconditioning or postconditioning mimics ischemic preconditioning or ischemic postconditioning. Recent small clinical trial demonstrated the cardioprotective effect of remote ischemic preconditioning and morphine during primary PCI. But this study was small and did not demonstrate the separate effect of morphine-induced cardioprotection. 2. Study Objective To investigate the effects of ticagrelor on myocardial infarct size in patients with STEMI undergoing primary PCI compared with clopidogrel To investigate the effects of morphine-induced cardioprotection during primary PCI in patients with STEMI

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
ST-Segment Elevation Myocardial Infarction

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Ticagrelor + Intracoronary Morphine
Arm Type
Experimental
Arm Description
180 mg loading pre-PCI followed by 90 mg bid for 5 days. Intracoronary Morphine Sulfate 3 mg + Saline 3 ml mix.
Arm Title
Ticagrelor + Intracoronary Saline
Arm Type
Experimental
Arm Description
180 mg loading pre-PCI followed by 90 mg bid for 5 days. Saline 3 ml intracoronary injection.
Arm Title
Clopidogrel + Intracoronary Morphine
Arm Type
Experimental
Arm Description
600 mg loading pre-PCI followed by 75 mg qd for 5 days. Morphine Sulfate 3 mg + Saline 3 ml mix intracoronary injection.
Arm Title
Clopidogrel + Intracoronary Saline
Arm Type
Active Comparator
Arm Description
600 mg loading pre-PCI followed by 75 mg qd for 5 days. Saline 3 ml intracoronary injection.
Intervention Type
Drug
Intervention Name(s)
Ticagrelor
Other Intervention Name(s)
Brilinta
Intervention Type
Drug
Intervention Name(s)
Clopidogrel
Other Intervention Name(s)
Plavix
Intervention Type
Drug
Intervention Name(s)
Morphine Sulfate
Other Intervention Name(s)
Morphine
Intervention Type
Drug
Intervention Name(s)
Saline
Other Intervention Name(s)
Normal Saline
Primary Outcome Measure Information:
Title
Myocardial infarct size measured by magnetic resonance imaging (MRI) at 3-5 days after the index procedure
Time Frame
Post-PCI 3-5 days
Secondary Outcome Measure Information:
Title
Rate of complete ST-segment resolution on ECG obtained 30 minutes after the procedure
Time Frame
30 min after completion of PCI
Title
Enzymatic Infarct size by creatine kinase-MB (area under curve)
Time Frame
1 month later
Title
Myocardial salvage index measured by MRI
Time Frame
Post-PCI 3-5 days
Title
Major adverse cardiac events (a composite of death, myocardial infarction, severe heart failure, or stent thrombosis)
Time Frame
1Month later
Title
The extent of microvascular obstruction measured by MRI
Time Frame
post-PCI 3-5days
Title
The number of segments with >75% of infarct transmurality measured by MRI
Time Frame
post-PCI 3-5 days
Title
The presence of myocardial hemorrhage measured by MRI
Time Frame
post-PCI 3-5 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria Subject must be at least 20 years of age. Patients undergoing primary PCI for STEMI Diagnosis of STEMI: ST-segment elevation >0.1 millivolt in ≥2 contiguous leads or (presumably) new left bundle branch block Presence of symptoms less than 12 hours Additional inclusion criteria for intracoronary morphine TIMI flow grade 0 or 1 of infarct related arteries Exclusion Criteria: Known hypersensitivity or contraindication to study medications or contrast Female of childbearing potential, unless a recent pregnancy test is negative, who possibly plan to become pregnant any time after enrollment into this study. Rescue PCI after thrombolysis or facilitated PCI Cardiogenic shock or cardiopulmonary resuscitation before randomization Known chronic hepatic disease Known renal dysfunction (creatinine level 3.0mg/dL or dependence on dialysis). Decompensated chronic obstructive pulmonary disease or active asthma at inclusion Mechanical ventilation at inclusion Brain injury or intracranial hypertension Acute alcohol intoxication Known ulcerative colitis Active epilepsy Contraindications to undergo MRI imaging include any of the following A cardiac pacemaker or implantable defibrillator; any implanted or magnetically activated device; or any history indicating contraindication to MRI including claustrophobia or allergy to gadolinium Current use of oral anticoagulant An increased risk of bradycardia Sinus node dysfunction, atrioventricular dysfunction, or heart rate <40/min Patients receiving clopidogrel 300 mg or more before randomization One of followings history of intracranial bleeding intracranial tumor, arteriovenous malformation or aneurysm stroke within past 3 months Active bleeding of internal organ or bleeding diathesis Acute aortic dissection
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hyeon-Cheol Gwon, MD/PhD
Phone
82-2-3410-6653
Email
hcgwon62@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Joo-Yong Hahn, MD/PhD
Phone
82-2-3410-6653
Email
jyhahn@skku.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hyeon-Cheol Gwon, MD/PhD
Organizational Affiliation
Samsung Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Samsung Medical Center
City
Seoul
State/Province
Gang nam-Gu, Ilwon-Dong
ZIP/Postal Code
135-710
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hyeon-Cheol Gwon, PhD
Phone
82-2-3410-6653
Email
hcgwon@skku.edu
First Name & Middle Initial & Last Name & Degree
Joo-Yong Hahn, PhD
Phone
82-2-3410-6653
Email
jy.hahn@samsung.com

12. IPD Sharing Statement

Citations:
PubMed Identifier
28427585
Citation
Kim EK, Park TK, Yang JH, Song YB, Choi JH, Choi SH, Chun WJ, Choe YH, Gwon HC, Hahn JY. Ticagrelor Versus Clopidogrel on Myocardial Infarct Size in Patients Undergoing Primary Percutaneous Coronary Intervention. J Am Coll Cardiol. 2017 Apr 25;69(16):2098-2099. doi: 10.1016/j.jacc.2017.02.034. No abstract available.
Results Reference
derived
PubMed Identifier
28373244
Citation
Gwag HB, Kim EK, Park TK, Lee JM, Yang JH, Song YB, Choi JH, Choi SH, Lee SH, Chang SA, Park SJ, Lee SC, Park SW, Jang WJ, Lee M, Chun WJ, Oh JH, Park YH, Choe YH, Gwon HC, Hahn JY. Cardioprotective Effects of Intracoronary Morphine in ST-Segment Elevation Myocardial Infarction Patients Undergoing Primary Percutaneous Coronary Intervention: A Prospective, Randomized Trial. J Am Heart Assoc. 2017 Apr 3;6(4):e005426. doi: 10.1161/JAHA.116.005426.
Results Reference
derived

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Ticagrelor and Intracoronary Morphine in Patients Undergoing Primary Percutaneous Coronary Intervention

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