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Clinical Trial Summary

The primary objective is to assess the effect of an oat ingredient provided over 4 weeks on serum LDL cholesterol in men and women with elevated LDL-cholesterol compared to a placebo.

Secondary endpoints are fasting serum total- and HDL-cholesterol, non-HDL-cholesterol, triglycerides, glucose, insulin, glycated albumin, HOMA-IR and Framingham risk score


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03911427
Study type Interventional
Source PepsiCo Global R&D
Contact
Status Completed
Phase N/A
Start date April 10, 2019
Completion date February 28, 2020

See also
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