Effect of ingestion of yacon syrup in huma
- Conditions
- AppetiteWomenF02.830.071M01.975
- Registration Number
- RBR-33wf46
- Lead Sponsor
- Fundação Universidade Estadual do Ceará FUNECE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- Female
- Target Recruitment
- Not specified
Women; between 20 and 40 years old; do not present chronic self-reported diseases; have a body mass index of eutrophy or obesity grade I; regular menstrual cycle.
Pregnancy or lactation; hysterectomy performed; current smoker or in the last 30 days; users of illicit drugs; daily consumption of ethanol higher than 15g; current or last 30 days use of hypoglycemic, lipid-lowering, antibiotic and anti-inflammatory medications, laxatives or weight-loss medications; have inflammatory diseases such as inflammatory bowel disease (Crohn's disease, ulcerative colitis); endocrinopathy carrier’s (cushing's syndrome, hypothyroidism), cancer carrier’s, having celiac disease or lactose intolerance; have constipation history; present current consumption and in the last 30 days of fiber and fructooligosaccharides supplementation.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Improvement of the postprandial response of the plasma biomarkers of appetite after ingestion of yacon syrup compared to placebo;verified by blood dosage of glucagon-like peptide 1 (GLP1) and ghrelin at times 0, 15, 30, 45, 60, 90, 120 and 180. The improvement will be verified if there is statistical significance (p <0.05) in the comparison of the areas under the curve between treatment A (syrup intake) and treatment B (placebo intake), a difference of at least 50% between treatments is expected.
- Secondary Outcome Measures
Name Time Method Improvement of the postprandial response of serum glycemia, serum insulin, serum triglycerides and subjective sensation of satiety after yacon syrup ingestion compared to placebo; verified by glucose, insulin and triglycerides blood dosages and self-reporting on satiety at times 0, 15, 30, 45, 60, 90, 120 and 180. The improvement will be verified if there is statistical significance (p <0, 05) in the comparison of the areas under the curve between treatment A (syrup intake) and treatment B (placebo intake), a difference of at least 50% between treatments is expected.