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The Effect of Spice Consumption on Postprandial Vascular Function

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03063320
Enrollment
43
Registered
2017-02-24
Start date
2017-01-25
Completion date
2020-02-26
Last updated
2023-09-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Risk Factor

Brief summary

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.

Detailed description

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.

Interventions

OTHERSpice blend

Test spices include cardamom, coriander, cumin, ginger, paprika, red pepper, turmeric, cinnamon

Sponsors

Penn State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

Person assessing the outcome measures will be blinded to participant allocation

Intervention model description

3 period randomized cross over

Eligibility

Sex/Gender
ALL
Age
30 Years to 75 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Change in flow mediated dilationChange from baseline at 2 hours and 4 hours after meal consumptionEndothelial function measured by FMD

Secondary

MeasureTime frameDescription
Lipid and lipoproteinsChange from baseline during the 4 hours after meal consumptionTotal cholesterol, LDL cholesterol, HDL cholesterol, Triglycerides
Plasma Inflammatory cytokinesChange from baseline during the 4 hours after meal consumptionSerum: IL-1β, IL-6, IL-10, IL-12p70, interferon-gamma, monocyte chemoattractant protein-1, macrophage inflammatory protein-1alpha, TNF-alpha, vascular endothelial growth factor
Inflammatory cytokines in isolated peripheral blood mononuclear cellsChange from baseline during the 4 hours after meal consumptionTNF-alpha, IL-6,NF-κB, I-κB, MAP kinase, COX-2, iNOS from stimulated and unstimulated lipopolysaccharides in peripheral blood mononuclear cells. Activation status of macrophages.
GlucoseChange from baseline during the 4 hours after meal consumptionPlasma glucose
InsulinChange from baseline during the 4 hours after meal consumptionPlasma insulin
Plasma antioxidantsChange from baseline during the 4 hours after meal consumptionhydrophilic ORAC, lipophilic ORAC, total ORAC

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026