Overweight and Obesity Clinical Trial
Official title:
Effects of Juice Plus+® Supplementation on Endothelial Function in Overweight Men: A Randomized, Controlled Trial
Verified date | August 2011 |
Source | Griffin Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
The purpose of the study is to determine the effects of daily ingestion of Juice Plus+® capsules containing Orchard, Garden and Vineyard blends on endothelial function and biomarkers of oxidative stress (oxidized LDL, lipid hydroperoxides and protein carbonyls) in overweight men as compared to the placebo group.
Status | Completed |
Enrollment | 70 |
Est. completion date | August 2010 |
Est. primary completion date | July 2010 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 18 Years to 75 Years |
Eligibility |
Inclusion Criteria: 1. Male age 25-75 years 2. Healthy (no known diabetes mellitus, cardiovascular disease, or eating disorder) 3. Non-smoker 4. Overweight (BMI =25) with central adiposity as indicated by waist circumference (=102 cm). 5. Endothelial dysfunction with high-fat meal Exclusion Criteria: 1. Use of lipid-lowering or antihypertensive medications, unless stable on medication for at least 3 months and willing to refrain from taking medication for 12 hours prior to EF scanning; 2. Regular use of multivitamins and/or complementary or alternative supplement therapy (including all Juice Plus+® products) and unwillingness to discontinue supplementation for at least 8 weeks prior to study initiation and for study duration 3. Anticipated inability to complete or comply with study protocol; 4. Diagnosed eating disorder 5. Any rheumatologic disease requiring regular use of NSAIDs or alternative medications 6. Regular use of fiber supplements 7. Use of insulin, glucose sensitizing medication, or vasoactive medication 8. Substance abuse (chronic alcoholism, or other chemical dependency 9. Pre-existing cardiovascular disease. |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
United States | Yale-Griffin Prevention Research Center | Derby | Connecticut |
Lead Sponsor | Collaborator |
---|---|
Griffin Hospital | NSA, LLC |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Endothelial Function | Brachial artery flow mediated dilation (FMD) | 8 weeks | No |
Secondary | Weight | 8 weeks | No | |
Secondary | Waist Circumference | 8 weeks | No | |
Secondary | Blood pressure | 8 weeks | No | |
Secondary | Serum biomarker measures | These samples will be used to assess participants' biomarkers of oxidative stress (i.e. oxidized LDL levels, lipid hydroperoxides, and protein carbonyls) and compliance measure (i.e. serum carotenoids) | 8 weeks | No |
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