Healthy, Postmenopausal Women Clinical Trial
— RZNOfficial title:
Effects of CabernayZyns (Dried Cabernet Grapes) Intake on Vascular Function and Platelet Reactivity in Postmenopausal Women
Verified date | October 2017 |
Source | University of California, Davis |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study assesses the acute effects of dried Cabernet grape intake on vascular function and platelet reactivity in postmenopausal women. Previous studies from this lab and others have demonstrated acute effects on vascular function and platelet reactivity from phenolic-rich food sources. Postmenopausal women are suggested as the study group, as they are likely to have compromised vascular function due to the loss of protective estrogen, and have been the study group for past and present research projects in this lab.
Status | Completed |
Enrollment | 20 |
Est. completion date | July 2017 |
Est. primary completion date | April 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 50 Years to 70 Years |
Eligibility |
Inclusion Criteria: - Postmenopausal female: 50-70 years - Women: lack of menses for at least one year and FSH 23-116.3 mlU/mL - Subject is willing and able to comply with the study protocols. - Subject is willing to participate in all study procedures - BMI 25.0 - 40 kg/m2 - Weight = 110 pounds Exclusion Criteria: - BMI = 40 kg/m2 - Dislike or allergy for grape products and raisins - Self-reported use of daily anticoagulation agents including aspirin, NSAIDs - Vegan, Vegetarians, food faddists or those consuming a non-traditional diet - Alcohol consumption > 3 drinks/week (i.e. 1 bottle of beer, 1 glass of wine, and 1 shot of hard liquor) - Fruit consumption = 2 cups/day - Vegetable consumption = 3 cups/day for females - Fatty Fish = 3 times/week - Coffee/tea = 3 cups/day - Dark chocolate = 3 oz/day - Self-reported restriction of physical activity due to a chronic health condition - Self-reported chronic/routine high intensity exercise - Self-reported diabetes - Blood pressure = 140/90 mm Hg - Self-reported renal or liver disease - Self-reported heart disease, which includes cardiovascular events and stroke - Inability to properly place or wear the PAT probes or abnormal measurements on pre-screening PAT - Abnormal Liver, CBC or Chemistry panels (laboratory values outside the reference range) if determined to be clinically significant by the study physician. - Self-reported cancer within past 5 years - Self-reported malabsorption - Currently taking prescription drugs or supplements. - Use of multi-vitamin and mineral other than a general formula of vitamins and minerals that meet the RDA - Not willing to stop any supplement use, including herbal, plant or botanical, fish oil, oil supplements a month prior to study enrollment. - Indications of substance or alcohol abuse within the last 3 years - Screening LDL = 190 mg/dl for those who have 0-1 major risk factors apart from LDL cholesterol (i.e. family history of premature coronary artery disease (male first degree relative < 55 years; CHD in female first degree relative < 65 years), cigarette smoker, HDL-C = 40 mg/dL]. - Screening LDL = 160 mg/dl for those who have 2 major risk factors apart from LDL cholesterol [i.e. family history of premature coronary artery disease (male first degree relative < 55 years; CHD in female first degree relative < 65 years), cigarette smoker, HDL-C = 40 mg/dL]. (using NCEP calculator http://cvdrisk.nhlbi.nih.gov/calculator.asp); - Screening LDL = 130 mg/dl for those who have 2 major risk factors apart from LDL cholesterol [i.e. family history of premature coronary artery disease (male first degree relative < 55 years; CHD in female first degree relative < 65 years), cigarette smoker, HDL-C = 40 mg/dL], and a Framingham 10-year Risk Score 10-20% (using NCEP calculator http://cvdrisk.nhlbi.nih.gov/calculator.asp). - Current enrollee in a clinical research study. The following special populations will be excluded: - Individuals who are not yet adults (infants, children, teenagers) - Pregnant women - Prisoners |
Country | Name | City | State |
---|---|---|---|
United States | Ragle Human Nutrition Center | Davis | California |
Lead Sponsor | Collaborator |
---|---|
University of California, Davis |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Postprandial Micro-vascular Function | To determine whether an acute intake of dried Cabernet grapes will improve vascular function, as measured using peripheral artery tonometry (PAT). | Baseline and 2-hour measures on day 0 and day 7. | |
Secondary | Platelet Aggregation | To determine whether an acute intake of dried Cabernet grapes will alter platelet reactivity, as measured by Chrono-log platelet aggregometer device. | Baseline and 2-hour measures on day 0 and day 7. | |
Secondary | Nitrate/Nitrite | Blood analysis to determine whether an acute intake of dried Cabernet grapes will affect plasma circulating nitrate and nitrite levels. | Baseline and 2-hour measures on day 0 and day 7. | |
Secondary | Baseline Complete Metabolic Panel | Blood analyses will include measurements of complete blood cell count, comprehensive metabolic panel, and lipid profile. | Baseline measures on day 0 and day 7. | |
Secondary | Postprandial Complete Metabolic Panel | Blood analyses will include measurements of complete blood cell count, comprehensive metabolic panel, and lipid profile. | 2-hour measures on day 0 and day 7. | |
Secondary | Body Weight | Body weight will be recorded at baseline on initial visit as well as visit one week after. | Baseline measure on day 0 and day 7. | |
Secondary | Blood Pressure | The office blood pressure measurement will be obtained (3 measurements 5 minutes apart after a 15 minute rest). | Baseline measure on day 0 and day 7. |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT02950402 -
Dried Plums and Chronic Disease Markers
|
N/A |