Skip to main content
Clinical Trials/NCT00930956
NCT00930956CompletedNot Applicable

Resistant Starch Type 2 and Cross Linked Resistant Starch Type 4 on Blood Glucose

Kansas State University1 site in 1 country11 target enrollmentStarted: May 1, 2006Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
11
Locations
1
Primary Endpoint
Blood glucose

Study Overview

Brief Summary

This study is to determine whether different types of resistant starch have different effects on blood glucose in healthy adults.

Detailed Description

Each volunteer will visit the laboratory in a 10-12 hour fasted state on three occasions over a three-week period, up to two visits/wk, with at least 48 hours between visits. Volunteers will be asked to refrain from vigorous physical activity and the consumption of alcohol the day before each testing visit. Randomization using a Latin Square design was applied to minimize confounding issues associated with the order of administration.

In the morning of each test, a finger-prick capillary blood samples will be collected to determine fasting (baseline) blood glucose levels. The volunteers will then consume the test solution assigned for that trial. Ten minutes will be allowed for the test solution to be consumed. Over the two hours following the start of each test, finger-prick capillary blood samples were collected at 30, 60, 90, and 120 min. Blood glucose levels will be immediately measured in duplicate using an automated blood glucose analyzer (YSI 2300, Yellow Springs, OH). Analysis of the collected sample was repeated if the difference between duplicate samples was greater than 0.1 mmol/L. Once the samples were analyzed, the data was entered and the incremental area under the curve was calculated using the trapezoidal model (GraphPad v5.0, La Jolla, CA).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Prevention
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 35 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •apparently healthy

Exclusion Criteria

  • •diagnosis of any chronic disease
  • •wheat allergy

Arms & Interventions

Dextrose

Active Comparator

30 g of carbohydrate via Sun-Dex OGTT beverage

Intervention: Resistant Starch (Dietary Supplement)

RS Type 2

Experimental

30g Resistant Starch Type 2 (Hi-Maize 260, National Starch)

Intervention: Resistant Starch (Dietary Supplement)

RS Type 4 (cross linked)

Experimental

30g of cross linked RS type 4 (Fibersym RW, MGP Ingredients, Inc.)

Intervention: Resistant Starch (Dietary Supplement)

Outcomes

Primary Outcomes

Blood glucose

Time Frame: Acute response -- fasting and 30, 60, 90 and 120 minutes post-ingestion

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other

Study Sites (1)

Loading locations...

Similar Trials