Hyperglycemia
Conditions
Interventions
This is a randomized, controlled, two-arm, crossover clinical trial conducted with 18 participants diagnosed with type 2 diabetes mellitus, in which all participants were allocated to receive both int
Sponsors
Universidade Federal de Goiás
Universidade Federal de Goiás
Eligibility
Age
20 Years to 50 Years
Inclusion criteria
Inclusion criteria: Individuals aged 20 to 50 years; both sexes; diagnosed with type 2 diabetes mellitus; under medical supervision and using a stable dose of oral hypoglycemic agents for at least six months
Exclusion criteria
Exclusion criteria: Pregnant women; individuals with dietary restrictions or participants in dietary restriction programs; individuals with autoimmune diseases, hepatic or renal diseases, or infectious diseases; individuals with food allergies; use of anti-inflammatory drugs, antibiotics, immunosuppressive agents, or nutritional supplements; chronic alcohol users; failure to complete all study assessments
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome 1: A reduction in glucose levels is expected at 60 minutes after the meal, considering a minimum variation of 10% between groups;Observed outcome 1: A reduction of 34.4% in postprandial glucose concentration was observed at 60 minutes after the meal, comparing the intervencione;Expected Outcome 2: A reduction in the postprandial glucose area under the curve (AUC) is expected, considering a minimum difference of 10% between interventions;Observed Outcome 2: A 37.4% reduction in the postprandial glucose area under the curve (AUC) was observed between the interventions. | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes were expected. | — |
Countries
Brazil
Contacts
Public ContactJoão Mota
Universidade Federal de Goiás
Outcome results
None listed