Appetitive Behavior, Blood Pressure, Potential Abnormality of Glucose Tolerance
Conditions
Keywords
Crocus sativus, Blood glucose responses, blood pressure, subjective appetite, blood glucose concentrations
Brief summary
This study investigated the effects of two different doses of Crocus Sativus in glucose beverages on glycemic responses.
Detailed description
This study examined the short-term effects of two different doses (15 mg and 30 mg) of Crocus Sativus in glucose beverages on postprandial glycemic responses in healthy young adults.
Interventions
Eleven healthy subjects (male: 6, female: 5) after 10-14h fast, consumed 50 g D-glucose, three times, in different weeks along with 250 mL water; and 50 g D-glucose containing 15 mg and 30 mg of Crocus Sativus tested once, in different weeks along with 250 mL water. Fingertip capillary blood glucose samples were taken at 0, 15, 30, 45, 60, 90 and 120 min postmeal. The first glucose sample was taken exactly 15 min after the beginning of the consumption of the tested beverage.
Eleven healthy subjects (male: 6, female: 5) after 10-14h fast, consumed 50 g D-glucose, three times, in different weeks along with 250 mL water; and 50 g D-glucose containing 15 mg and 30 mg of Crocus Sativus tested once, in different weeks along with 250 mL water. Fingertip capillary blood glucose samples were taken at 0, 15, 30, 45, 60, 90 and 120 min postmeal. The first glucose sample was taken exactly 15 min after the beginning of the consumption of the tested beverage.
Eleven healthy subjects (male: 6, female: 5) after 10-14h fast, consumed 50 g D-glucose, three times, in different weeks along with 250 mL water; and 50 g D-glucose containing 15 mg and 30 mg of Crocus Sativus tested once, in different weeks along with 250 mL water. Fingertip capillary blood glucose samples were taken at 0, 15, 30, 45, 60, 90 and 120 min postmeal. The first glucose sample was taken exactly 15 min after the beginning of the consumption of the tested beverage.
Sponsors
Study design
Masking description
A researcher not involved in data analyses was responsible for participant allocation and test food consumption.
Intervention model description
Crossover, double blind, randomized clinical trial
Eligibility
Inclusion criteria
* Healthy * Non-smoking * Non-diabetic men and women * Body Mass Index (BMI) between 18.5 and 24.9 kg/m2 * Normal blood pressure
Exclusion criteria
* Severe chronic disease (e.g., coronary heart disease, diabetes mellitus, kidney or liver conditions, endocrine conditions) * Gastrointestinal disorders * Pregnancy * Lactation * Competitive sports * Alcohol abuse * Drug dependency * Allergy in Crocus Sativus
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Capillary blood glucose responses | 2 hours | Clinically useful change in blood glucose, defined as the restoration of glucose within normal limits during the 2-hour oral glucose tolerance test |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Subjective appetite ratings | 2 hours | Useful change in subjective appetite using visual analogue scales with a score from 0 to 10 (given in the form of booklet, one scale per page) at baseline, 15, 30, 45, 60, 90 and 120 min. The minimum or maximum score will be evaluated if it is better or worse depending on the appetite variable e.g., hunger, satiety, desire to eat etc. |
| Blood pressure | 2 hours | Useful change in systolic and diastolic blood pressure before and 2-hour after consumption of the three beverages |
Countries
Greece