Olive Oil and Cardiovascular Health
Status: | Completed |
---|---|
Conditions: | Peripheral Vascular Disease, Hematology |
Therapuetic Areas: | Cardiology / Vascular Diseases, Hematology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 5/5/2014 |
Start Date: | December 2013 |
End Date: | December 2014 |
Contact: | Eric Bruhn |
Phone: | 507-255-7100 |
Effects of Hydroxytyrosol on Vascular Health
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).
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).
Subjects will be included if they have all of the following
1. Age ≥ 18 years old
2. Have known diagnosis of coronary artery disease
3. Demonstrated endothelial dysfunction (reactive hyperemia - EndoPAT score < 2.0) at
time of screening
Patient exclusion criteria:
Patients will be excluded if they have one or more of the following:
1. Hypertension (at Screening): any patient with systolic blood pressure (SBP) ≥ 170
mmHg or diastolic blood pressure ≥ 110 mmHg, or hypotension (SBP < 100 mmHg)
2. Uncontrolled Diabetes Mellitus
3. Experienced an acute coronary syndrome within 3 months
4. PCI or revascularization for an acute coronary syndrome within 3 months
5. Second (II) or third (III) degree heart block without a pacemaker and/or concurrent
potentially life threatening arrhythmia or other uncontrolled arrhythmia
6. Congestive heart failure NYHA class III and IV
7. Unstable serum creatinine (>2.0)
8. 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:
- History of major gastrointestinal tract surgery such as gastrectomy,
gastroenterostomy, or bowel resection
- Any history of pancreatic injury, pancreatitis or evidence of impaired
pancreatic function/injury as indicated by abnormal lipase or amylase
- Evidence of hepatic disease as determined by a history of hepatic
encephalopathy, a history of cirrhosis, esophageal varices, or a history of
portocaval shunt
9. Any concurrent life threatening condition with a life expectancy less than 2 years
10. History or evidence of drug or alcohol abuse within the last 12 months
11. 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
12. History of noncompliance to medical regimens or unwillingness to comply with the
study protocol
13. History of malignancy other than basal cell skin cancer within the past five years
14. 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
15. Use of other investigational drugs at the time of enrollment, or within 30 days or 5
half-lives of enrollment, whichever is longer
16. Any condition that in the opinion of the investigator would jeopardize the evaluation
of efficacy or safety
17. Persons directly involved in the execution of this protocol
18. Pregnant or nursing (lactating) women
19. 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
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