The Effect of Spice Consumption on Postprandial Vascular Function



Status:Completed
Conditions:Peripheral Vascular Disease
Therapuetic Areas:Cardiology / Vascular Diseases
Healthy:No
Age Range:30 - 75
Updated:3/24/2019
Start Date:January 25, 2017
End Date:December 31, 2018

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The Effect of Chronic Consumption of Popular Spices on Postprandial Vascular Function

A 3-period randomized cross-over, controlled feeding study will be conducted to determine the
effect of chronic spice consumption on postprandial vascular function. Participants will
consume three test diets containing different amounts of spice. Each treatment period will
last for 4 weeks. After each diet period a meal test will be conducted. Participants will
consume a meal with a spice content corresponding to the diet period they have just
completed. Endothelial function will be measured at 2 and 4 hours after meal consumption.
Blood samples will also be taken during the 4 hours after meal consumption for measurement of
lipids, immune and inflammatory markers.

A 3-period randomized cross-over, controlled feeding study will be conducted to determine the
effect of chronic spice consumption on postprandial vascular function, lipid levels, immune
and inflammatory markers. Participants will consume three test diets containing different
amounts of spice. Each treatment period will last for 4 weeks. At baseline and after each
diet period a postprandial test will be conducted. Flow mediated dilation (FMD) will
conducted in the fasting state and a catheter will be inserted for blood sampling.
Participants will consume a control test meal containing low spice at baseline and after each
diet period the test meal will contain a level of spice that corresponds to the amount of
spice consumed during the diet period. Blood samples will be taken at 30, 60, 120, 180 and
240 minutes after meal consumption, and FMD will be performed at 120 and 240 minutes.

Inclusion Criteria:

Men and postmenopausal women Overweight or obese (25-35kg/m2) Non-smoking Waist
circumference >= 94cm for men and >=80cm for women

At least one other of the following:

- LDL- cholesterol >130mg/dL

- CRP >1mg/L

- Triglycerides >=150mg/dL

- HDL <40mg/dL for men or <50mg/dL for women

- Systolic blood pressure >= 130mmHg or diastolic >= 85mmHg

- Fasting glucose >=100mg/dL

Exclusion Criteria:

- Diabetes (fasting glucose >126mg/dL)

- Hypertension (systolic blood pressure >160mmHg or diastolic blood pressure >100mmHg)

- Prescribed anti-hypertensive or glucose lowering drugs

- Established cardiovascular disease, stroke, diabetes, liver, kidney or autoimmune
disease

- Use of cholesterol/lipid lowering medication or supplementation (psyllium, fish oil,
soy lecithin, phytoestrogens) and botanicals

- Pregnancy or lactation

- Weight loss of >=10% of body weight within the 6 months prior to enrolling in the
study

- Vegetarianism
We found this trial at
1
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University Park, Pennsylvania 16802
Phone: 814-863-8622
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University Park, PA
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