Postprandial Glycemia Clinical Trial
Official title:
A Randomized, Controlled, Double-blind, Cross-over Clinical Trial, Evaluating the Effect of MealShape™ on the Postprandial Glycemia After Eating Standard Food, in Healthy Volunteers.
The purpose of the study is to evaluate the effect of MealShape, a Ceylon cinnamon extract (Cinnamomum zeylanicum) on blood glucose and insulin response after consumption of a standard meal composed of white bread, in healthy male and female volunteers.
Status | Completed |
Enrollment | 18 |
Est. completion date | February 2014 |
Est. primary completion date | February 2014 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 45 Years |
Eligibility |
Inclusion Criteria: - Healthy male and female volunteers, able to read and write, aged from 18 to 45 years inclusive at time of screening - Good physical condition - Body Mass Index (BMI) = 18,5 and < 25 kg/m² - Written informed consent provided prior to screening, after receiving and understanding the subject information - Stable body weight (< 5% variation) within the last 3 months prior to screening. - Subject accepting to keep the same lifestyle throughout the study regarding physical activity, no smoking etc. - Registered with the French Social Security, in agreement with the French law on biomedical experimentation. Exclusion Criteria: - Subject with type 1 or 2 diabetes - Smoker. Light smoker (less than 5 cigarettes per day) or former smoker (smoking more than 5 cigarettes per day) having stopped less than three months. Smoking (or use of smoking substitute e.g. nicotine patch) is not permitted from screening throughout the study. - Subject with fasting capillary blood glucose level > 110 mg/dl. - Subject with fasting capillary blood glucose level = 110 mg/dl and 2 hours postprandial capillary blood glucose level > 140 mg/dl during an Oral Glucose Tolerance Test. - Subject with any sensitivity or allergy to any of the products used within this clinical trial. - Intake of product (food and dietary supplement) having an effect on glycemia and insulinemia. - Intake of all chronic medication excepted oestroprogestative or progestative contraception started at least three months preceding the screening visit. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
France | Centre de Nutrition Clinique Naturalpha | Lilles |
Lead Sponsor | Collaborator |
---|---|
Dialpha |
France,
Baker WL, Gutierrez-Williams G, White CM, Kluger J, Coleman CI. Effect of cinnamon on glucose control and lipid parameters. Diabetes Care. 2008 Jan;31(1):41-3. Epub 2007 Oct 1. — View Citation
Davis PA, Yokoyama W. Cinnamon intake lowers fasting blood glucose: meta-analysis. J Med Food. 2011 Sep;14(9):884-9. doi: 10.1089/jmf.2010.0180. Epub 2011 Apr 11. Review. — View Citation
Finkelstein EA, Khavjou OA, Thompson H, Trogdon JG, Pan L, Sherry B, Dietz W. Obesity and severe obesity forecasts through 2030. Am J Prev Med. 2012 Jun;42(6):563-70. doi: 10.1016/j.amepre.2011.10.026. — View Citation
Magistrelli A, Chezem JC. Effect of ground cinnamon on postprandial blood glucose concentration in normal-weight and obese adults. J Acad Nutr Diet. 2012 Nov;112(11):1806-9. doi: 10.1016/j.jand.2012.07.037. — View Citation
Rafehi H, Ververis K, Karagiannis TC. Controversies surrounding the clinical potential of cinnamon for the management of diabetes. Diabetes Obes Metab. 2012 Jun;14(6):493-9. doi: 10.1111/j.1463-1326.2011.01538.x. Epub 2011 Dec 27. Review. — View Citation
Zimmet P, Alberti KG, Shaw J. Global and societal implications of the diabetes epidemic. Nature. 2001 Dec 13;414(6865):782-7. Review. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Blood glucose incremental Area Under the Curve between 0 and 120 minutes after consumption of a standard meal, compared between MealShape and the placebo | Over 120 minutes after the consumption of a standard meal | No | |
Secondary | Blood glucose incremental Area Under the Curve between 0 and 60 minutes compared between MealShape and the placebo after consumption of a standard meal, | Over 60 minutes after consumption of a standard meal | No | |
Secondary | Capillary blood glucose maximal concentration between MealShape and Placebo after consumption of a standard meal | Over 120 minutes after consumption of a standard meal | No | |
Secondary | Comparison of glycemia values between MealShape and Placebo at the following time points: T0, T15, T30, T45, T60, T90 and T120 minutes after consumption of a standard meal | Over 120 minutes after consumption of a standard meal | No | |
Secondary | Evaluation of the safety of MealShape with adverse events recording | 3 weeks | Yes | |
Secondary | Insulin incremental Area under the Curve between 0 and 120 minutes compared between MealShape and Placebo after consumption of a standard meal | Over 120 minutes after consumption of a standard meal | No | |
Secondary | Insulin incremental Area under the Curve between 0 and 60 minutes compared between MealShape and Placebo after consumption of a standard meal | Over 60 minutes after connsumption of a standard meal | No |
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