Clinical Trials Directory

Trials / Completed

CompletedNCT02161250

Effects of Resistant Starch in a Beverage on Post-prandial Glycemic and Insulinemic Responses

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Purdue University · Academic / Other
Sex
All
Age
18 Years – 29 Years
Healthy volunteers
Accepted

Summary

Hypothesis: A beverage with a resistant starch will blunt and sustain the post-prandial rise in blood glucose and insulin concentrations compared to beverage with maltodextrin (an easily digested carbohydrate).

Detailed description

* About two-thirds of adults in the United States are overweight or obese which can cause adverse health consequences for those individuals. Post-prandial hyperglycemia is one of these possible consequences and is associated with a higher risk for Type 2 Diabetes. Controlling hyperglycemia is important in the prevention of the onset of diabetes and obesity. Resistant starch is a dietary carbohydrate which is not completely digested in the gut and produces energy for the body to use. The investigators are interested in assessing the effects of resistant starch on postprandial blood glucose and insulin concentrations. * Aim: To assess the effects of a resistant starch on post-prandial blood glucose and insulin concentrations. * Hypothesis: A beverage with a resistant starch will blunt and sustain the post-prandial rise in blood glucose and insulin concentrations compared to a beverage with maltodextrin (an easily digested carbohydrate).

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTResistant StarchEach subject will complete 2 testing days (randomized and crossover design). On each of 2 test days, subjects will arrive at the Purdue Clinical Research Center after a 12-h fast and will consume a beverage containing resistant starch. The test beverage will be consumed along with a standard meal provided at the start of the test day. A second standard meal that does not contain the beverage will be consumed four hours later. Below is what will be included in the test bar.
DIETARY_SUPPLEMENTControlEach subject will complete 2 testing days (randomized and crossover design). On each of 2 test days, subjects will arrive at the Purdue Clinical Research Center after a 12-h fast and will consume a beverage containing maltodextrin. The test beverage will be consumed along with a standard meal provided at the start of the test day. A second standard meal that does not contain the beverage will be consumed four hours later. Below is what will be included in the test bar.

Timeline

Start date
2014-04-01
Primary completion
2014-05-01
Completion
2014-06-01
First posted
2014-06-11
Last updated
2014-06-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02161250. Inclusion in this directory is not an endorsement.