Resistant Starch Type 2 and Cross Linked Resistant Starch Type 4 on Blood Glucose
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Kansas State University
- 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
30 g of carbohydrate via Sun-Dex OGTT beverage
Intervention: Resistant Starch (Dietary Supplement)
RS Type 2
30g Resistant Starch Type 2 (Hi-Maize 260, National Starch)
Intervention: Resistant Starch (Dietary Supplement)
RS Type 4 (cross linked)
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
