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

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
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
NCT ID
NCT02901379
First Posted
September 6, 2016
Last Updated
August 22, 2018
Sponsor
National Cardiovascular Center Harapan Kita Hospital Indonesia
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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