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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01308892
Other study ID # NL33506.081.10
Secondary ID
Status Completed
Phase N/A
First received February 15, 2011
Last updated June 16, 2011
Start date January 2011
Est. completion date June 2011

Study information

Verified date June 2011
Source Wageningen University
Contact n/a
Is FDA regulated No
Health authority Netherlands: Medical Ethics Review Committee (METC)Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)
Study type Interventional

Clinical Trial Summary

In the CHOC study the investigators will examine the effect of chocolate flavanols on vascular function, inflammation, oxidative stress and markers of endothelial function. The effects of both acute consumption and prolonged consumption will be studied. The secondary objectives are to investigate if daily intake of chocolate flavanols for 4 weeks will improve the response to a high fat/high energy challenge.


Recruitment information / eligibility

Status Completed
Enrollment 44
Est. completion date June 2011
Est. primary completion date June 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 45 Years to 70 Years
Eligibility Inclusion Criteria:

- Male

- 45-70 years old

- BMI between 25 and 32 kg/m2

Exclusion Criteria:

- Urine glucose concentrations outside normal ranges (> 0,25 g/l)

- Fasting blood glucose < 7.0 mmol/L)

- Systolic Bp > 160 mmHg or diastolic Bp > 100 mmHg

- Blood Hb values below 8.4 mmol/L

- Allergic to cow milk, dairy products or chocolate

- Vegetarian

- Tobacco smoker

- Diagnosed with any long-term medical condition (e.g., diabetes, hemophilia, cardiovascular disease, anemia, gastrointestinal disease, renal failure)

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator)


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
High flavanol chocolate
chocolate high in flavanols
Low flavanol chocolate
chocolate low in flavanols
High fat challenge
Milkshake with 95g fat

Locations

Country Name City State
Netherlands Wageningen universiteit division of human Wageningen Gelderland

Sponsors (2)

Lead Sponsor Collaborator
Wageningen University Top Institute Food and Nutrition

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Blood pressure 0, 4wk No
Primary FMD 0, 4wk No
Primary PWA 0, 4wk No
Secondary leukocyte count and activation 0, 4wk No
Secondary PBMC gene expression 0, 4wk No
Secondary Markers of inflammation and ED 0, 4wk No
Secondary Blood pressure acute study part 0 and 2h No
Secondary FMD acute study part 0 and 2hrs No
Secondary PWA acute study part 0 and 2 hrs No
Secondary Leukocyte count and activation acute study part 0 and 2 hrs No
Secondary PBMC gene expression acute study part 0 and 2 hrs No
Secondary markers of inflammation and ED acute study part 0 and 2hrs No
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