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The purpose of this study is to conduct a double-blind, randomized controlled trial (RCT), to determine if six month supplementation of olive oil can improve the health of the blood vessels and improve long term health of the heart and blood vessels, in patients requiring percutaneous coronary intervention (PCI).
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Inclusion and exclusion criteria
Subjects will be included if they have all of the following
Patient exclusion criteria:
Patients will be excluded if they have one or more of the following:
Hypertension (at Screening): any patient with systolic blood pressure (SBP) ≥ 170 mmHg or diastolic blood pressure ≥ 110 mmHg, or hypotension (SBP < 100 mmHg)
Uncontrolled Diabetes Mellitus
Experienced an acute coronary syndrome within 3 months
PCI or revascularization for an acute coronary syndrome within 3 months
Second (II) or third (III) degree heart block without a pacemaker and/or concurrent potentially life threatening arrhythmia or other uncontrolled arrhythmia
Congestive heart failure NYHA class III and IV
Unstable serum creatinine (>2.0)
Any surgical or medical condition which might significantly alter the absorption, distribution, metabolism, or excretion of the olive oil including, but not limited to, any of the following:
Any concurrent life threatening condition with a life expectancy less than 2 years
History or evidence of drug or alcohol abuse within the last 12 months
History of hypersensitivity to any of the study drugs or to medications belonging to the same therapeutic class as the study drugs as well as known or suspected contraindications to the study drugs
History of noncompliance to medical regimens or unwillingness to comply with the study protocol
History of malignancy other than basal cell skin cancer within the past five years
Any surgical or medical condition, which in the opinion of the investigator, may place the patient at higher risk from his/her participation in the study, or is likely to prevent the patient from complying with the requirements of the study or completing the study
Use of other investigational drugs at the time of enrollment, or within 30 days or 5 half-lives of enrollment, whichever is longer
Any condition that in the opinion of the investigator would jeopardize the evaluation of efficacy or safety
Persons directly involved in the execution of this protocol
Pregnant or nursing (lactating) women
Women of child-bearing potential unless postmenopausal for at least one year, surgically sterile or using effective methods of contraception as defined by local Health Authorities
Primary purpose
Allocation
Interventional model
Masking
0 participants in 2 patient groups, including a placebo group
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Data sourced from clinicaltrials.gov
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