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Effect of 80-mg Atorvastatin on Myocardial Edema

Primary Purpose

Myocardial Edema

Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Atorvastatin 80mg
Atorvastatin 10mg
Sponsored by
National Cardiovascular Center Harapan Kita Hospital Indonesia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Myocardial Edema focused on measuring atorvastatin, myocardial edema, Follistatin-like 1, FSTL1, atorvastatin 80mg, coronary artery bypass surgery

Eligibility Criteria

40 Years - 65 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with coronary artery disease indicated for CABG surgery
  • has signed informed consent

Exclusion Criteria:

  • high risk EURO (European System for Cardiac Operative Risk Evaluation) score
  • creatinin value>2 g/dl
  • direct bilirubin value >3 mg/ml
  • AST/ALT (aspartate transaminase / alanine transaminase) value >1,5 times UNL (upper normal limit)
  • high pre-operative CKMB (Creatine Kinase-MB) and troponin
  • LVEF (Left Ventricular Ejection Fraction) <45%
  • concomitant valve disease required surgery
  • contraindicated for MRI
  • high degree ventricular arrhytmia
  • coagulation disorder
  • COPD (chronic obsructive pulmonary disease)
  • HIV (Human Immunodeficiency Virus) +, HBV (Hepatitis B Virus)+, HCV (Hepatitis C Virus) +
  • conduction abnormality, pacemaker
  • electrolyte or blood gas disturbance
  • receiving immunosuppressive drug or cytotoxic agent 4 weeks before surgery
  • receiving macrolide, azole antifungal, fibrate, or protease inhibitor HIV drug

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Atorvastatin 80mg

    Atorvastatin 10mg

    Arm Description

    Subjects who will receive atorvastatin 80mg for two weeks

    Subject who will receive atorvastatin 10mg

    Outcomes

    Primary Outcome Measures

    T2 relaxation time
    T2 relaxation time (in ms) difference between control and study group

    Secondary Outcome Measures

    FSTL1 plasma level
    FSTL1 plasma level difference between control and study group
    PKA plasma level
    PKA plasma level difference between control and study group
    PKB plasma level
    PKB plasma level difference between control and study group
    hs-CRP plasma level
    hs-CRP plasma level difference between control and study group
    MDA plasma level
    MDA plasma level difference between control and study group
    Change from baseline FSTL1 plasma level
    Change from baseline PKA plasma level
    Change from baseline PKB plasma level

    Full Information

    First Posted
    September 6, 2016
    Last Updated
    August 22, 2018
    Sponsor
    National Cardiovascular Center Harapan Kita Hospital Indonesia
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02901379
    Brief Title
    Effect of 80-mg Atorvastatin on Myocardial Edema
    Official Title
    Effect of 80-mg Atorvastatin on Myocardial Edema Following Coronary Artery Bypass Surgery in Relation With Follistatin-Like Protein-1
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2018
    Overall Recruitment Status
    Completed
    Study Start Date
    October 2016 (undefined)
    Primary Completion Date
    August 2018 (Actual)
    Study Completion Date
    August 2018 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    National Cardiovascular Center Harapan Kita Hospital Indonesia

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The purpose of this study is to determine whether atorvastatin 80mg can reduce the development of myocardial edema following coronary artery bypass surgery. This study also want to determine: whether atorvastatin 80mg can influence Follistatin-like 1 (FSTL1) plasma level following bypass surgery? whether there is correlation between myocardial edema and FSTL1 plasma level? the efficacy of atorvastatin 80mg compared to atorvastatin 10mg in reducing hs-CRP (high sensitive-C reactive protein) and MDA (malondialdehyde) plasma level following bypass surgery? the efficacy of atorvastatin 80mg compared to atorvastatin 10mg in raising PKA and PKB plasma level following bypass surgery?
    Detailed Description
    This study is an double blinded experimental study using parallel design. Study subjects are patients in Harapan Kita hospital who are registered to CABG (Coronary Artery Bypass Graft) surgery and fulfill all the eligibility criteria. The subjects will be first consecutively selected, with male age 40-65 as the criteria. After that the investigators do the randomization with block randomization method. All the subjects will be given drug with label A and label B (only the pharmacist know the which dose of atorvastatin belong to which label). Total subjects needed for this study are 30 (15 belong to study group and 15 belong to control group) MRI (Magnetic Resonance Imaging) results will be read by two radiologists, and analyzed using cronbach alpha. The results are considered equal if the cronbach >0,7. If it is proven to be unequal, then the third radiologist will decide. Statin is known to have several adverse effects, such as myopathy, myositis to rhabdomyolysis, elevated liver enzyme, memory loss, GI (gastrointestinal) disturbance, and severa others. Therefore, the investigators will check baseline CK (creatine kinase) and liver enzyme at the beginning of the study, before the surgery, and if the patient feel any symptoms. Statin will be stopped if patient decide to stop, or if there is increase in ALT (alanine aminotransferase) higher that three time upper normal value, or if there is increase in CK higher than ten times upper normal value. Statistical analysis using IBM SPSS statistics version 21.0. Comparative analysis for variables such as smoking history, obesity, hypertension, dyslipidemia, diabetes, family history, infarct history, ACE-I/ARB (angiotensin converting enzyme inihibitor /angiotensin receptor blocker) therapy will be using chi-square or fischer. Comparative analysis for variables T2 relaxation time, FSTL1, hs-CRP, PKA (protein kinase A), PKB (Protein Kinase B), MDA, age, CPB (Cardiopulmonary Bypass) time, CABG time will using unpaired t-test or Mann-whitney. Correlative analysis between FSTL1 and T2 relaxation time will be using Pearson test.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Myocardial Edema
    Keywords
    atorvastatin, myocardial edema, Follistatin-like 1, FSTL1, atorvastatin 80mg, coronary artery bypass surgery

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare ProviderInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    40 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Atorvastatin 80mg
    Arm Type
    Experimental
    Arm Description
    Subjects who will receive atorvastatin 80mg for two weeks
    Arm Title
    Atorvastatin 10mg
    Arm Type
    Active Comparator
    Arm Description
    Subject who will receive atorvastatin 10mg
    Intervention Type
    Drug
    Intervention Name(s)
    Atorvastatin 80mg
    Other Intervention Name(s)
    Lipitor
    Intervention Description
    Subject will be given atorvastatin 80mg for two weeks
    Intervention Type
    Drug
    Intervention Name(s)
    Atorvastatin 10mg
    Other Intervention Name(s)
    Lipitor
    Intervention Description
    Subjects will be give atorvastatin 10mg as part of standard therapy in hospital
    Primary Outcome Measure Information:
    Title
    T2 relaxation time
    Description
    T2 relaxation time (in ms) difference between control and study group
    Time Frame
    day 6 after CABG
    Secondary Outcome Measure Information:
    Title
    FSTL1 plasma level
    Description
    FSTL1 plasma level difference between control and study group
    Time Frame
    day 6 after CABG
    Title
    PKA plasma level
    Description
    PKA plasma level difference between control and study group
    Time Frame
    day 6 after CABG
    Title
    PKB plasma level
    Description
    PKB plasma level difference between control and study group
    Time Frame
    day 6 after CABG
    Title
    hs-CRP plasma level
    Description
    hs-CRP plasma level difference between control and study group
    Time Frame
    day 1 after CABG
    Title
    MDA plasma level
    Description
    MDA plasma level difference between control and study group
    Time Frame
    day 1 after CABG
    Title
    Change from baseline FSTL1 plasma level
    Time Frame
    day 1 and day 6 after CABG
    Title
    Change from baseline PKA plasma level
    Time Frame
    day 1 and day 6 after CABG
    Title
    Change from baseline PKB plasma level
    Time Frame
    day 1 and day 6 after CABG

    10. Eligibility

    Sex
    Male
    Minimum Age & Unit of Time
    40 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients with coronary artery disease indicated for CABG surgery has signed informed consent Exclusion Criteria: high risk EURO (European System for Cardiac Operative Risk Evaluation) score creatinin value>2 g/dl direct bilirubin value >3 mg/ml AST/ALT (aspartate transaminase / alanine transaminase) value >1,5 times UNL (upper normal limit) high pre-operative CKMB (Creatine Kinase-MB) and troponin LVEF (Left Ventricular Ejection Fraction) <45% concomitant valve disease required surgery contraindicated for MRI high degree ventricular arrhytmia coagulation disorder COPD (chronic obsructive pulmonary disease) HIV (Human Immunodeficiency Virus) +, HBV (Hepatitis B Virus)+, HCV (Hepatitis C Virus) + conduction abnormality, pacemaker electrolyte or blood gas disturbance receiving immunosuppressive drug or cytotoxic agent 4 weeks before surgery receiving macrolide, azole antifungal, fibrate, or protease inhibitor HIV drug
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Rita Zahara
    Organizational Affiliation
    National Cardiovascular Center Harapan Kita
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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    Effect of 80-mg Atorvastatin on Myocardial Edema

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