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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03542240
Other study ID # HM20012060
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 19, 2018
Est. completion date November 13, 2020

Study information

Verified date January 2021
Source Virginia Commonwealth University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will investigate the effects of curcumin on the structure/function of the body by investigating whether targeted improvement of intestinal barrier function by supplementation with oral curcumin will result in attenuation of lipopolysaccharide (LPS) translocation and/or intestinal inflammation.


Description:

A typical diet in the United States, also known as Western diet, is very high in sugars and saturated fat, and poor in food such as fruits, vegetables, fish and whole grains. This type of diet is associated with higher risk to develop obesity and other health problems such as high blood pressure, high cholesterol, Type 2 diabetes, and heart disease. Western diet can also cause changes in the gut that allow bacteria that are typically only present in the gut to leak out into the bloodstream. It is thought that having gut bacteria in the bloodstream may play a role in the development of diseases like Type 2 diabetes and heart disease. Curcumin is a dietary supplement that comes from the root of the turmeric plant, and it may have an effect on the function of the gut and the leakage of gut bacteria into the bloodstream. The purpose of this research study is to evaluate the effects of daily curcumin dietary supplements on the function of the gut in subjects who are at risk for cardiovascular and metabolic diseases, for example they have increased blood pressure, increase waist circumference and high triglycerides (fat in the blood).


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date November 13, 2020
Est. primary completion date November 13, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Based on National Institutes of Health (NIH) definition of Metabolic syndrome, the subject must meet at least 3 of the following criteria: A. Waist Circumference: Female = 88 cm, Male = 102 cm B. Blood Pressure: = 130/85 mm/Hg and/or treatment with blood pressure lowering medication C. Impaired fasting glucose or HbA1c (fasting glucose = 100 mg/dl or HgA1c = 5.7 D. HDL-C: Females< 50 mg/dl, Males < 40 mg/dl E. Triglycerides = 150 mg/dl 2. Willing and able to comply with the study protocol Exclusion Criteria: 1. Diabetes 2. Established cardiovascular disease 3. Pre-existing liver disease other than NAFLD 4. Chronic kidney disease (Stage 4 and 5) 5. Rheumatological disease 6. Active malignancy 7. Alcohol consumption greater than 7 drinks per week for females and greater than 14 drinks per week for males 8. Current use of metformin and/or steroids 9. Curcumin supplementation 10. Females of child-bearing potential (NOT of child-bearing potential is defined as s/p hysterectomy or post-menopausal.) 11. Prisoners/wards of the state and individuals with limited English proficiency

Study Design


Intervention

Dietary Supplement:
Curcumin
500 milligram daily supplement

Locations

Country Name City State
United States Virginia Commonwealth University Richmond Virginia

Sponsors (1)

Lead Sponsor Collaborator
Virginia Commonwealth University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change inintestinal permeability Measured by level plasma lipopolysaccharide (LPS). A reduction in LPS suggests a reduction in intestinal permeability Baseline to 12 months
Primary Change in intestinal barrier function Measured by level of excreted Zonulin in stool samples. A reduction in Zonulin suggests a reduction in intestinal barrier function Baseline to 12 months
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