Metabolic Syndrome
Conditions
Interventions
This is a randomized, controlled, two-arm, double-blind clinical trial. Participants will be included in the experimental group or in the control group if they are aged 18 years or older, of both sexe
G07.203.300.456
Sponsors
Centro Universitário Cesmac
Centro Universitário Cesmac
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Adults of either sex who have at least three of the five following items: waist above 102 cm in men and above 88 cm in women; triglycerides above 150mg/dL; HDL cholesterol below 40 mg/dL for men and below 50 mg/dL for women; blood pressure above 130/85 mmHg; fasting blood glucose above 110 mg/dL
Exclusion criteria
Exclusion criteria: Pregnant women; lactating women; allergic to any component of the supplement dry extract of red propolis; cancer patients; chronic renal patients; psychiatric patients
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find differences in measures of total cholesterol, LDL and HDL cholesterol, glycated hemoglobin (HBA1C) and fasting blood glucose after the interventional period of 60 days. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to find differences in insulin measurements, ALT and AST liver enzymes, triglycerides and C-reactive protein after the interventional period of 60 days. | — |
Countries
Brazil
Contacts
Public ContactMilena Meireles
Centro Universitário Cesmac
Outcome results
None listed