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Evaluation of the Effect of SGLT-2 Inhibitors on Cardiac Remodeling in Post Myocardial Infarction Patients

Primary Purpose

Myocardial Infarction, Diabetes Mellitus, Type 2, Myocardial Remodeling, Ventricular

Status
Recruiting
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Dapagliflozin 10Mg Tab
Sponsored by
Ain Shams University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Myocardial Infarction focused on measuring Dapagliflozin, ST2, Myocardial infarction, Cardiac remodeling, T2DM

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Female or male aged >18 and < 75 years
  2. Diabetic post myocardial infarction patients
  3. First anterior STEMI with successful TIMI-3 flow
  4. STEMI within 12 hrs of onset of chest pain
  5. creatine clearance ≥60 mL/min
  6. HbA1c between 6.5% and 12.0%

Exclusion Criteria:

  1. Cardiogenic shock on admission
  2. Multivessel disease on admission
  3. Mechanical complications e.g. mitral regurge on admission
  4. Life threatening arrhythmia on admission
  5. Hemodynamic instability on admission
  6. Diagnosis of Type 1 diabetes mellitus
  7. History of bladder cancer or history of radiation therapy to the lower abdomen or pelvis at any time
  8. Active urinary infection diagnosed by clinical symptoms of urgency and frequency + lab tests
  9. Pregnant or breast-feeding patients
  10. Active participation in another clinical study
  11. AST or ALT >3x ULN or Total bilirubin >2.5 x ULN
  12. CrCl < 60 ml/min (based on the Cockroft-Gault equation)

Sites / Locations

  • Ain shams university hospitalsRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Intervention arm

Control arm

Arm Description

30 patients will receive standard of care in addition to the SGLT2 Dapagliflozin 10 mg daily for 4 Weeks Interventions: Drug: Dapagliflozin 10 mg oral tablets Standard of care: Dual antiplatelet therapy, Statin, anticoagulation therapy

30 patients will receive standard of care (Dual antiplatelet therapy, Statin, anticoagulation therapy) for 4 weeks

Outcomes

Primary Outcome Measures

Effect on ST2 (suppression of tumerogenicity 2) level in the acute phase after myocardial infarction
patients will be followed up for the whole period of the study and blood sample will be drawn at baseline and at study end to track changes in the level of ST2 (suppression of tumerogenicity 2) which is a cardiac remodeling biomarker using ELISA technique

Secondary Outcome Measures

Echocardiographic changes due to intervention
patients will have their echocardiography and ejection fraction will be compared at baseline and at the end of the study to track any changes that may be caused by intervention

Full Information

First Posted
March 28, 2022
Last Updated
September 20, 2022
Sponsor
Ain Shams University
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1. Study Identification

Unique Protocol Identification Number
NCT05335629
Brief Title
Evaluation of the Effect of SGLT-2 Inhibitors on Cardiac Remodeling in Post Myocardial Infarction Patients
Official Title
Evaluation of the Effect of Dapagliflozin on Cardiac Remodeling in Post Myocardial Infarction Patients
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2022 (Actual)
Primary Completion Date
September 2023 (Anticipated)
Study Completion Date
September 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ain Shams 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

5. Study Description

Brief Summary
A prospective, randomized, controlled study will be conducted at Clinical Cardioglogy department, Ain Shams University Hospitals, assessing the efficacy and tolerability of SGLT2 inhibitors (dapagliflozin) addition on the clinical outcome and cardiac remodeling markers of post myocardial infarction (MI) diabetic patients
Detailed Description
All patients presenting to the Clinical Cardiology department, Ain Shams University Hospitals, will be assessed for eligibility as follow: Inclusion criteria: Female or male aged >18 and < 75 years Diabetic post myocardial infarction patients First anterior STEMI with successful TIMI-3 flow STEMI within 12 hrs of onset of chest pain creatine clearance ≥60 mL/min HbA1c between 6.5% and 12.0% Exclusion criteria: Cardiogenic shock on admission Multivessel disease on admission Mechanical complications e.g. mitral regurge on admission Life threatening arrhythmia on admission Hemodynamic instability on admission Diagnosis of Type 1 diabetes mellitus History of bladder cancer or history of radiation therapy to the lower abdomen or pelvis at any time Active urinary infection diagnosed by clinical symptoms of urgency and frequency + lab tests Pregnant or breast-feeding patients Active participation in another clinical study AST or ALT >3x ULN or Total bilirubin >2.5 x ULN CrCl < 60 ml/min (based on the Cockroft-Gault equation) Eligible patients will be randomly assigned into one of 2 arms: Group 1 (Healthy control) (n=10) Aged-matched healthy volunteers who do not suffer any diseases. Group 2 (Control group) (n= 30): Post-MI patients who will receive standard of care for 4 Weeks Group 3 (Test group) (n= 30): Post-MI patients who will receive standard of care in addition to the SGLT2 Dapagliflozin 10 mg daily for 4 Weeks Dapagliflozin will be administered immediately at time of PCI and daily for 4 weeks. Standard of care will given to both arms (group 2 and 3) and includes: Dual Antiplatelet Therapy (DAPT), high intensity statin, anticoagulation therapy, ACEI or aldosterone antagonist depending on the ejection fraction All subjects will sign an informed consent statement prior to inclusion in the study. All subjects will be followed up for 4 weeks and blood samples will be withdrawn at baseline, 1 week, and the end of the study to test for ST2 (suppression of tumerogenicity 2) biomarker

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myocardial Infarction, Diabetes Mellitus, Type 2, Myocardial Remodeling, Ventricular
Keywords
Dapagliflozin, ST2, Myocardial infarction, Cardiac remodeling, T2DM

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention arm
Arm Type
Active Comparator
Arm Description
30 patients will receive standard of care in addition to the SGLT2 Dapagliflozin 10 mg daily for 4 Weeks Interventions: Drug: Dapagliflozin 10 mg oral tablets Standard of care: Dual antiplatelet therapy, Statin, anticoagulation therapy
Arm Title
Control arm
Arm Type
No Intervention
Arm Description
30 patients will receive standard of care (Dual antiplatelet therapy, Statin, anticoagulation therapy) for 4 weeks
Intervention Type
Drug
Intervention Name(s)
Dapagliflozin 10Mg Tab
Intervention Description
Dapagliflozin is a sodium-glucose cotransporter-2 inhibitor (SGLT2 inhibitor) which is a new class of hypoglycemic drugs, and they can block sodium-dependent glucose transporter-2 (SGLT2) located in the early proximal renal tubule to increase urinary glucose excretion and decrease the concentration of blood glucose
Primary Outcome Measure Information:
Title
Effect on ST2 (suppression of tumerogenicity 2) level in the acute phase after myocardial infarction
Description
patients will be followed up for the whole period of the study and blood sample will be drawn at baseline and at study end to track changes in the level of ST2 (suppression of tumerogenicity 2) which is a cardiac remodeling biomarker using ELISA technique
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
Echocardiographic changes due to intervention
Description
patients will have their echocardiography and ejection fraction will be compared at baseline and at the end of the study to track any changes that may be caused by intervention
Time Frame
4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Female or male aged >18 and < 75 years Diabetic post myocardial infarction patients First anterior STEMI with successful TIMI-3 flow STEMI within 12 hrs of onset of chest pain creatine clearance ≥60 mL/min HbA1c between 6.5% and 12.0% Exclusion Criteria: Cardiogenic shock on admission Multivessel disease on admission Mechanical complications e.g. mitral regurge on admission Life threatening arrhythmia on admission Hemodynamic instability on admission Diagnosis of Type 1 diabetes mellitus History of bladder cancer or history of radiation therapy to the lower abdomen or pelvis at any time Active urinary infection diagnosed by clinical symptoms of urgency and frequency + lab tests Pregnant or breast-feeding patients Active participation in another clinical study AST or ALT >3x ULN or Total bilirubin >2.5 x ULN CrCl < 60 ml/min (based on the Cockroft-Gault equation)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Abdallah Heshmat, Bachelor of Pharmacy
Phone
01025526964
Email
Abdullahheshmat.azzam@gmail.com
Facility Information:
Facility Name
Ain shams university hospitals
City
Cairo
Country
Egypt
Individual Site Status
Recruiting

12. IPD Sharing Statement

Plan to Share IPD
No
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Evaluation of the Effect of SGLT-2 Inhibitors on Cardiac Remodeling in Post Myocardial Infarction Patients

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