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NCT03844503: RS

Food Containing Resistant Starch Type 4 and Postprandial Glycemic Response

Completed NA Last updated 14 July 2020
What this trial tests

NA trial testing Cereal Bar no fiber in Healthy in 31 participants. Completed in 25 October 2019.

Timeline
11 February 2019
Primary endpoint
25 October 2019
25 October 2019

Quick facts

Lead sponsorClinical Nutrition Research Center, Illinois Institute of Technology
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingsingle
Primary purposebasic science
Enrollment31
Start date11 February 2019
Primary completion25 October 2019
Estimated completion25 October 2019
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Clinical Nutrition Research Center, Illinois Institute of Technology — full company profile →

Who can join

Adults 20 to 45, any sex, with Healthy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary objective of the study is to determine if resistant starch reduces the 2 hour glycemic response as measured by positive incremental area under the blood glucose response curve (Positive iAUC- ignores area below fasting). Secondary endpoints include insulin iAUC, glucose and insulin net incremental AUC (net iAUC), time point of peak rise (T max) of glucose and insulin, and glucose and insulin concentrations at each time point (C max).

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Healthy

Currently open trials in the same condition.

Other Clinical Nutrition Research Center, Illinois Institute of Technology trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03844503.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing