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Comparison of Different Types of Resistant Starch

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00930956
Enrollment
11
Registered
2009-07-02
Start date
2006-05-31
Completion date
2009-05-31
Last updated
2010-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postprandial Hyperglycemia

Keywords

Diabetes, Obesity, Hyperglycemia, Dietary Fiber, Wheat, Grain

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).

Interventions

DIETARY_SUPPLEMENTResistant Starch

30 g of carbohydrate per Arm

Sponsors

Kansas State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* apparently healthy

Exclusion criteria

* diagnosis of any chronic disease * wheat allergy

Design outcomes

Primary

MeasureTime frame
Blood glucoseAcute response -- fasting and 30, 60, 90 and 120 minutes post-ingestion

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026