Effect of Resistant Starch Type 4 on Glycemia and Insulin Sensitivity in Young Adults
This study has been completed.
Sponsor:
Kansas State University
Collaborator:
MGP Ingredients, Inc
Information provided by:
Kansas State University
ClinicalTrials.gov Identifier:
NCT00687960
First received: May 22, 2008
Last updated: May 28, 2008
Last verified: May 2008
| Tracking Information | |||||
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| First Received Date ICMJE | May 22, 2008 | ||||
| Last Updated Date | May 28, 2008 | ||||
| Start Date ICMJE | November 2006 | ||||
| Primary Completion Date | May 2007 (final data collection date for primary outcome measure) | ||||
| Current Primary Outcome Measures ICMJE |
Post-Prandial Metabolism [ Time Frame: Early morning ] [ Designated as safety issue: No ] | ||||
| Original Primary Outcome Measures ICMJE | Same as current | ||||
| Change History | Complete list of historical versions of study NCT00687960 on ClinicalTrials.gov Archive Site | ||||
| Current Secondary Outcome Measures ICMJE | Not Provided | ||||
| Original Secondary Outcome Measures ICMJE | Not Provided | ||||
| Current Other Outcome Measures ICMJE | Not Provided | ||||
| Original Other Outcome Measures ICMJE | Not Provided | ||||
| Descriptive Information | |||||
| Brief Title ICMJE | Effect of Resistant Starch Type 4 on Glycemia and Insulin Sensitivity in Young Adults | ||||
| Official Title ICMJE | Effect of Resistant Starch Type 4 on Glycemia and Insulin Sensitivity in Young Adults | ||||
| Brief Summary | This study tested the effects of resistant starch type 4 on blood sugar and hunger in young adults with Type 2 diabetes. |
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| Detailed Description | To measure the blood glucose response, after an overnight fast, blood samples were collected before eating and at 15, 30, 45, 60, 90, and 120 minutes after each each bar. The incremental area under the curve was used to calculate the glycemic index and insulin sensitivity via minimal model. |
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| Study Type ICMJE | Interventional | ||||
| Study Phase | Not Provided | ||||
| Study Design ICMJE | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Crossover Assignment Masking: Double Blind (Subject, Outcomes Assessor) Primary Purpose: Supportive Care |
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| Condition ICMJE | Hyperglycemia | ||||
| Intervention ICMJE |
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| Study Arm (s) |
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| Publications * | Not Provided | ||||
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||
| Recruitment Status ICMJE | Completed | ||||
| Enrollment ICMJE | 13 | ||||
| Completion Date | December 2007 | ||||
| Primary Completion Date | May 2007 (final data collection date for primary outcome measure) | ||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||
| Ages | 18 Years to 35 Years | ||||
| Accepts Healthy Volunteers | Yes | ||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
| Location Countries ICMJE | United States | ||||
| Administrative Information | |||||
| NCT Number ICMJE | NCT00687960 | ||||
| Other Study ID Numbers ICMJE | KSU-HML-RSt2 | ||||
| Has Data Monitoring Committee | No | ||||
| Responsible Party | Mark Haub Ph.D., Department of Human Nutrition | ||||
| Study Sponsor ICMJE | Kansas State University | ||||
| Collaborators ICMJE | MGP Ingredients, Inc | ||||
| Investigators ICMJE |
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| Information Provided By | Kansas State University | ||||
| Verification Date | May 2008 | ||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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