Flavanol-Rich Cocoa and Cerebral Blood Flow
This study is ongoing, but not recruiting participants.
Sponsor:
Brigham and Women's Hospital
Collaborator:
MasterFoods
Information provided by (Responsible Party):
Naomi DL Fisher, MD, Brigham and Women's Hospital
ClinicalTrials.gov Identifier:
NCT00825695
First received: January 20, 2009
Last updated: April 20, 2012
Last verified: April 2012
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Purpose
The purpose of the study is to learn whether or not cocoa has a beneficial effect on blood flow to the brain in older subjects with diabetes mellitus or hypertension (high blood pressure). We hypothesize that cocoa, which contains flavanols (a type of polyphenol), may help to promote blood flow to the brain in older people with diabetes or hypertension.
| Condition | Intervention |
|---|---|
|
Hypertension Diabetes |
Dietary Supplement: cocoa |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Investigator, Outcomes Assessor) Primary Purpose: Prevention |
| Official Title: | Flavanol-Rich Cocoa, Vascular Responses and Mechanisms |
Resource links provided by NLM:
Further study details as provided by Brigham and Women's Hospital:
Primary Outcome Measures:
- functional transcranial doppler measures [ Time Frame: 1 month ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 66 |
| Study Start Date: | January 2009 |
| Estimated Study Completion Date: | December 2013 |
| Estimated Primary Completion Date: | September 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Active Comparator: flavanol-rich cocoa |
Dietary Supplement: cocoa
two servings of cocoa daily for one month
Other Name: Cocoa Pro
|
| Placebo Comparator: flavanol-poor cocoa |
Dietary Supplement: cocoa
two servings of cocoa daily for one month
Other Name: Cocoa Pro
|
Eligibility| Ages Eligible for Study: | 65 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- diabetes and/or hypertension
Exclusion Criteria:
- alzheimers disease, dementia, stroke, recent angina or heart attack
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00825695
Locations
| United States, Massachusetts | |
| Brigham and Women's Hospital | |
| Boston, Massachusetts, United States, 02115 | |
Sponsors and Collaborators
Brigham and Women's Hospital
MasterFoods
Investigators
| Principal Investigator: | Naomi D. Fisher, MD | Brigham and Women's Hospital |
More Information
No publications provided
| Responsible Party: | Naomi DL Fisher, MD, Principal Investigator, Brigham and Women's Hospital |
| ClinicalTrials.gov Identifier: | NCT00825695 History of Changes |
| Other Study ID Numbers: | P-001936, 1RO1HL089570 |
| Study First Received: | January 20, 2009 |
| Last Updated: | April 20, 2012 |
| Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
|
Hypertension Vascular Diseases Cardiovascular Diseases |
ClinicalTrials.gov processed this record on June 18, 2013