Cardioprotection Clinical Trial
— ChocolateOfficial title:
Dark Chocolate and Cocoa Ingestion and Endothelial Function: A Randomized, Placebo Controlled, Cross-over Trial
NCT number | NCT00538083 |
Other study ID # | 2005-12 |
Secondary ID | |
Status | Completed |
Phase | Phase 1 |
First received | |
Last updated | |
Start date | August 2005 |
Est. completion date | May 2006 |
Verified date | March 2020 |
Source | Griffin Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Cardiovascular disease is the leading cause of death in the United States. Studies have shown
that obesity is an important risk factor for development of cardiovascular disease.
Endothelial dysfunction, a pathologic feature of obesity, predicts the occurrence of
cardiovascular disease. Recent research findings indicate that consumption of cocoa exerts
cardioprotective effects, which include increasing HDL levels, reduction in systolic BP,
inhibition of platelet aggregation/activity and activation of endothelial nitric oxide
synthase.
Proposed is a randomized controlled trial consisting of 4 phases designed to examine the
dose-response, and the acute and sustained effects of cocoa consumption on endothelial
function as a marker of cardiovascular disease risk in 45 otherwise healthy adults with a BMI
25-35kg/m2.
Status | Completed |
Enrollment | 45 |
Est. completion date | May 2006 |
Est. primary completion date | |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 30 Years to 75 Years |
Eligibility |
Inclusion Criteria: - Ages between 30 -75 - BMI between 25-35 kg/m2 - waist circumference above 88 cms. in women and 102 cms. in men - non-smoker - no strenuous exercise at least 8 hours prior to scanning - to facilitate recruitment individuals with diagnosed hypertension or hyperlipidemia will be included provided that they have been stable on their medications for three months, and can refrain from taking their medication 12 hours prior to BARS testing. Exclusion Criteria: - Failure to meet inclusion criteria - anticipated inability to complete study protocol for any reason - current eating disorder - diagnosed coronary artery disease - diabetes - sleep apnea - current or impending pregnancy - insulin or glucose sensitizing medication use, vasoactive medication or nutriceutical use (glucocorticoids, antineoplastic agents, psychoactive agents, or bronchodilators) - regular use of high dose vitamin E or C and unable to discontinue for duration of the study - regular use of fiber supplements and unable to discontinue for duration of the study - restricted diets by choice (i.e. vegan, Atkins diet etc) - allergy to cocoa or chocolate. |
Country | Name | City | State |
---|---|---|---|
United States | Griffin Hospital | Derby | Connecticut |
Lead Sponsor | Collaborator |
---|---|
Griffin Hospital | Centers for Disease Control and Prevention, The Hershey Company |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Endothelial Function(acute & sustained phase) | Single dose(acute phase), 6 weeks (sustained phase) | ||
Secondary | Blood Pressure(acute and sustained phase), lipid profile(sustained), LDL oxidation(sustained), lipid hydroperoxide(sustained), CRP(sustained), blood glucose(sustained), body weight(sustained), waist circumference(sustained), endothelin(sustained) | Single dose(acute phase), 6 weeks(sustained phase) |
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