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Clinical Trial Summary

The goal of this clinical trial is to determine the postprandial glycemic response of the two starches in humans. Participants will be asked to consume 2 test foods on 2 separate occasions and provide blood glucose samples over 120 minutes postprandial.


Clinical Trial Description

Enrolled participants who are generally healthy and free of major chronic conditions will be randomized to receive either Commercial Native Starch or Extrusion Processed Starch first and then will be crossed over to receive the opposite Intervention. The study will consist of two clinical test visits of 120 minutes separated by a washout period of at least 24 hours. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06048978
Study type Interventional
Source INQUIS Clinical Research
Contact
Status Completed
Phase N/A
Start date October 2, 2023
Completion date November 30, 2023

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