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The Effect of Early Administration of Dapagliflozin in STEMI Patients With LV Systolic Dysfunction

Primary Purpose

STEMI - ST Elevation Myocardial Infarction, Left Ventricular Systolic Dysfunction

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Dapagliflozin 10Mg Tab
Placebo
Sponsored by
Assiut University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

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

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 1st time STEMI within 24 hours undergoing PPCI. (Chest pain > 30 minutes and ST segment elevation in more than one lead, include the definition of MI with a reference: Third universal definition of MI. (published at ESC Clinical Practice Guidelines 2012).
  • LVEF less than 50%.
  • eGFR ≥20 mL/min/1.73 m2.

Exclusion Criteria:

  • Patients less than 18 years old.
  • T1D (Type I diabetes mellitus).
  • Hemodynamically unstable.
  • Cardiogenic shock (clinical syndrome of tissue hypoperfusion resulting from cardiac dysfunction).
  • History of chronic symptomatic HF with a prior hHF within last year
  • Patients on dialysis.
  • Serious hypersensitivity to dapagliflozin (eg, anaphylaxis, angioedema).
  • Pregnant or lactating women.
  • Sever hepatic impairment.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Placebo Comparator

    Arm Label

    dapagliflozin

    conventional therapy

    Arm Description

    (a) Dapagliflozin 10 mg once daily within 24 hours after PPCI for 3 month

    Reperfusion therapy: primary percutaneous coronary intervention (PPCI) after DAPT loading (aspirin 300 mg and either clopidogrel 600mg or ticagrelor 180 mg orally) in the ambulance or emergency department upon diagnosis. Anti-ischemic treatment: DAPT, SC-anticoagulation, beta blockers, statin or others will be individualized according to the patient condition. Anti-failure treatment: Angiotensin converting enzyme inhibitors or angiotensin II receptor blockers, beta blockers, mineralocorticoid receptor antagonists, other diuretics will be added in case of volume overload.

    Outcomes

    Primary Outcome Measures

    Echocardiographic parameter
    The improvement in the LVEF (≥ 5%) using biplane simpson method echocardiography

    Secondary Outcome Measures

    Changes in LV remodeling
    using echocardiography
    Changes in diastolic function
    using mitral Inflow Patterns electrocardiography
    Changes in LA volume index
    using by the biplane area-length method from apical 4- and 2-chamber views electrocardiography
    Changes in LV mass index.
    using by linear method electrocardiography
    Laboratory investigations.
    Changes of the NT-proBNP from baseline to 3 month follow up
    CV death and rehospitalization of HF
    Composite of CV death and rehospitalization of HF
    Individual component at composite end points.
    Composite of CV death or rehospitalization of HF
    ACS
    Reinfarction or readmission for ACS and target lesion revascularization.

    Full Information

    First Posted
    August 26, 2021
    Last Updated
    September 6, 2021
    Sponsor
    Assiut University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05045274
    Brief Title
    The Effect of Early Administration of Dapagliflozin in STEMI Patients With LV Systolic Dysfunction
    Official Title
    The Effect of Early Administration of Dapagliflozin in ST Elevation Myocardial Infarction Patients Presenting With Left Ventricular Systolic Dysfunction
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2021
    Overall Recruitment Status
    Unknown status
    Study Start Date
    December 2021 (Anticipated)
    Primary Completion Date
    June 2022 (Anticipated)
    Study Completion Date
    September 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Assiut University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    300 STIMI patients with LV systolic dysfunction will be divided into two equal groups (Group I (Study arm, n=150); will receive dapagliflozin plus conventional therapy and group (II) Control arm (n=150); will receive conventional therapy only to detect an improvement in the LVEF by ≥ 5
    Detailed Description
    300 STIMI patients with LV systolic dysfunction will be randomly divided into two equal groups (Group I (Study arm, n=150); will receive Reperfusion therapy: primary percutaneous coronary intervention (PPCI) after DAPT loading (aspirin 300 mg and either clopidogrel 600mg or ticagrelor 180 mg orally) in the ambulance or emergency department upon diagnosis. Anti-ischemic treatment: DAPT, SC-anticoagulation, beta blockers, statin or others will be individualized according to the patient condition. Anti-failure treatment: Angiotensin converting enzyme inhibitors or angiotensin II receptor blockers, beta blockers, mineralocorticoid receptor antagonists, other diuretics will be added in case of volume overload. Dapagliflozin: It will be given in a dose of 10 mg once daily within 24 hours after PPCI. Group (II) Control arm (n=150); will receive Reperfusion therapy: as in study arm Anti-ischemic treatment: as in study arm. Anti-failure treatment: as in study arm. LV echocardiographic analysis for both groups at baseline and 3 month follow up by 2D Echocardiography to assess: LVEF by simpson method Diastolic function LV diameter and volume. LA volume index. LV mass index. Severity of MR. Laboratory investigation substudy analysis: 50 patients from either group will undergo NT-proBNP at baseline and after 3 month follow up. Clinical outcomes: Patients will be followed up in a deducted outpatient clinic for assessment of clinical outcomes either by phone cell or clinic visits at 3 month. Patients will be assessed for the following clinical parameters: I. Composite of CV death and rehospitalization of HF. II. Individual component at composite end points. III. Reinfarction or readmission for ACS and target lesion revascularization. Research outcome measures: a. Primary (main): 1. The improvement in the LVEF (≥ 5%) using biplane simpson method echocardiography. a. Secondary (subsidiary): Echocardiographic parameters at 3 month follow up. Changes in LV remodeling. Changes in diastolic function Changes in LA volume index. Changes in LV mass index. Laboratory investigations. Changes of the NT-proBNP from baseline to 3 month follow up Clinical outcomes at 3month. I. Composite of CV death and rehospitalization of HF. II. Individual component at composite end points. III. Reinfarction or readmission for ACS and target lesion revascularization.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    STEMI - ST Elevation Myocardial Infarction, Left Ventricular Systolic Dysfunction

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Investigator
    Allocation
    Randomized
    Enrollment
    300 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    dapagliflozin
    Arm Type
    Active Comparator
    Arm Description
    (a) Dapagliflozin 10 mg once daily within 24 hours after PPCI for 3 month
    Arm Title
    conventional therapy
    Arm Type
    Placebo Comparator
    Arm Description
    Reperfusion therapy: primary percutaneous coronary intervention (PPCI) after DAPT loading (aspirin 300 mg and either clopidogrel 600mg or ticagrelor 180 mg orally) in the ambulance or emergency department upon diagnosis. Anti-ischemic treatment: DAPT, SC-anticoagulation, beta blockers, statin or others will be individualized according to the patient condition. Anti-failure treatment: Angiotensin converting enzyme inhibitors or angiotensin II receptor blockers, beta blockers, mineralocorticoid receptor antagonists, other diuretics will be added in case of volume overload.
    Intervention Type
    Drug
    Intervention Name(s)
    Dapagliflozin 10Mg Tab
    Other Intervention Name(s)
    aspirin 300 mg and either clopidogrel 600mg or ticagrelor 180 mg orally, DAPT, SC-anticoagulation, beta blockers, statin, Angiotensin converting enzyme inhibitors or angiotensin II receptor blockers, beta blockers, mineralocorticoid receptor antagonists, other diuretics will be added in case of volume overload.
    Intervention Description
    Dapagliflozin: It will be given in a dose of 10 mg once daily within 24 hours after PPCI. Reperfusion therapy: primary percutaneous coronary intervention (PPCI) after DAPT loading (aspirin 300 mg and either clopidogrel 600mg or ticagrelor 180 mg orally) in the ambulance or emergency department upon diagnosis. Anti-ischemic treatment: DAPT, SC-anticoagulation, beta blockers, statin or others will be individualized according to the patient condition. Anti-failure treatment: Angiotensin converting enzyme inhibitors or angiotensin II receptor blockers, beta blockers, mineralocorticoid receptor antagonists, other diuretics will be added in case of volume overload.
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo
    Other Intervention Name(s)
    aspirin 300 mg and either clopidogrel 600mg or ticagrelor 180 mg orally, DAPT, SC-anticoagulation, beta blockers, statin, Angiotensin converting enzyme inhibitors or angiotensin II receptor blockers, beta blockers, mineralocorticoid receptor antagonists, other diuretics will be added in case of volume overload.
    Intervention Description
    Reperfusion therapy: primary percutaneous coronary intervention (PPCI) after DAPT loading (aspirin 300 mg and either clopidogrel 600mg or ticagrelor 180 mg orally) in the ambulance or emergency department upon diagnosis. Anti-ischemic treatment: DAPT, SC-anticoagulation, beta blockers, statin or others will be individualized according to the patient condition. Anti-failure treatment: Angiotensin converting enzyme inhibitors or angiotensin II receptor blockers, beta blockers, mineralocorticoid receptor antagonists, other diuretics will be added in case of volume overload.
    Primary Outcome Measure Information:
    Title
    Echocardiographic parameter
    Description
    The improvement in the LVEF (≥ 5%) using biplane simpson method echocardiography
    Time Frame
    3 month follow up
    Secondary Outcome Measure Information:
    Title
    Changes in LV remodeling
    Description
    using echocardiography
    Time Frame
    3 month follow up
    Title
    Changes in diastolic function
    Description
    using mitral Inflow Patterns electrocardiography
    Time Frame
    3 month follow up
    Title
    Changes in LA volume index
    Description
    using by the biplane area-length method from apical 4- and 2-chamber views electrocardiography
    Time Frame
    3 month follow up
    Title
    Changes in LV mass index.
    Description
    using by linear method electrocardiography
    Time Frame
    3 month follow up
    Title
    Laboratory investigations.
    Description
    Changes of the NT-proBNP from baseline to 3 month follow up
    Time Frame
    3 month follow up
    Title
    CV death and rehospitalization of HF
    Description
    Composite of CV death and rehospitalization of HF
    Time Frame
    3 month follow up
    Title
    Individual component at composite end points.
    Description
    Composite of CV death or rehospitalization of HF
    Time Frame
    3 month follow up
    Title
    ACS
    Description
    Reinfarction or readmission for ACS and target lesion revascularization.
    Time Frame
    3 month follow up

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: 1st time STEMI within 24 hours undergoing PPCI. (Chest pain > 30 minutes and ST segment elevation in more than one lead, include the definition of MI with a reference: Third universal definition of MI. (published at ESC Clinical Practice Guidelines 2012). LVEF less than 50%. eGFR ≥20 mL/min/1.73 m2. Exclusion Criteria: Patients less than 18 years old. T1D (Type I diabetes mellitus). Hemodynamically unstable. Cardiogenic shock (clinical syndrome of tissue hypoperfusion resulting from cardiac dysfunction). History of chronic symptomatic HF with a prior hHF within last year Patients on dialysis. Serious hypersensitivity to dapagliflozin (eg, anaphylaxis, angioedema). Pregnant or lactating women. Sever hepatic impairment.

    12. IPD Sharing Statement

    Learn more about this trial

    The Effect of Early Administration of Dapagliflozin in STEMI Patients With LV Systolic Dysfunction

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