Pilot Study of the Effect of Purple Rice on Glucose Tolerance, Serum Lipids and Inflammation
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|ClinicalTrials.gov Identifier: NCT01720511|
Recruitment Status : Completed
First Posted : November 2, 2012
Last Update Posted : December 18, 2015
|Condition or disease||Intervention/treatment||Phase|
|Type 2 Diabetic||Dietary Supplement: Purple Rice Dietary Supplement: Brown Rice||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||10 participants|
|Intervention Model:||Crossover Assignment|
|Official Title:||Pilot Study of the Effect of Purple Rice on Glucose Tolerance, Serum Lipids and Inflammation.|
|Study Start Date :||September 2012|
|Actual Primary Completion Date :||October 2015|
|Actual Study Completion Date :||October 2015|
Experimental: Purple Rice
Twice a day given purple rice with 5mg of resveratrol.
Dietary Supplement: Purple Rice
Incorporate one cup of purple rice into dishes to be consumed at lunch and dinner each day for 4 weeks (equivalent of 4 ounces of uncooked rice/day).
Active Comparator: Brown RIce
Plain Purple rice given twice a day
Dietary Supplement: Brown Rice
Incorporate one cup of brown rice into dishes to be consumed at lunch and dinner each day for 4 weeks (equivalent of 4 ounces of uncooked rice/day).
- Glucose Tolerance [ Time Frame: 10 weeks ]Subjects will have an Intravenous line placed and fasting blood will be drawn. Subjects will then be given glucose to drink and blood will be drawn from an IV line for glucose and insulin.
- Serum Lipids [ Time Frame: 10 weeks ]Subjects will have an Intravenous line placed and fasting blood will be drawn for a chemistry-15 panel and High-sensitivity C-reaction Protein. Subjects will then be given 75 grams of glucose to drink and blood will be drawn from an IV line for glucose and insulin.
- Inflammation measured by highly sensitive C-reative protein test [ Time Frame: 10 weeks ]A high-sensitivity CRP (hs-CRP), that can be done in the lab using a blood test.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01720511
|United States, Louisiana|
|Pennington Biomedical Research Center|
|Baton Rouge, Louisiana, United States, 70808|