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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03329781
Other study ID # 200130089
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 2015
Est. completion date January 2018

Study information

Verified date April 2021
Source University of Glasgow
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Chronic diseases such as diabetes, cardiovascular diseases and cancer are a major burden on the Scottish population. Obesity and inflammation have strong links to these diseases. One of the mechanisms explaining the relationship between low-grade inflammation and excess weight is "endotoxaemia". We wish to study this phenomenon, when small components coming from our gut bacteria can pass into the bloodstream, raising the body's defences. Diet can modulate endotoxaemia. In this study, we propose to use curcumin, in a capsule form, to modulate endotoxaemia. Curcumin comes from turmeric, which is widely used as a spice. In this study, we want to test the effect of consuming curcumin extract to the composition of the gut microbiota, post-meal endotoxaemia, and inflammatory markers in blood.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date January 2018
Est. primary completion date January 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - BMI > 25 kg/m2. Exclusion Criteria: - having chronic inflammatory or autoimmune disease, gastrointestinal complaints or known biliary obstruction (past and present) - use of anti-inflammatory drugs 2 weeks before the start of the study - use of antibiotics during the 12 weeks preceding the trial - pregnancy - lactation

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
BCM-95
Consuming 1 capsule of BCM-95 per day.
Placebo
Consuming 1 placebo capsule per day

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Glasgow

Outcome

Type Measure Description Time frame Safety issue
Primary Level of endotoxin in plasma. 21 days
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