Subject with metabolic disorders such cardiovascular disease,
Conditions
Interventions
. The eligible subjects were randomized in two groups. One consumed propolis (n=35) and the other one (n=32) consume a placebo with same flavors and appearance than propolis (a mixture of peppermint a
45 and 90 days,
also they were controlled by phone interview,
focus group and personal interview along the study. All the analysis was made at day zero and ninety.
Propolis in human health
Sponsors
Fondos para la Innovación de la Competitividad (FIC) Maule Nº BIP.30.136.439-0
Fondos para la Innovación de la Competitividad (FIC) Maule Nº BIP.30.136.439-
0 and Rotterdam Labo
Eligibility
Sex/Gender
All
Age
0 Years to 0 Years
Inclusion criteria
Inclusion criteria: The inclusion criteria were: (1) age > 18 and < 69 years, (2) to have at least one of the following altered parameters: fast glycaemia, lipids profile, blood pressure, and/or over weight. To have some metabolism disorders like: diabetes mellitus, and cardiovascular disease.
Exclusion criteria
Exclusion criteria: The exclusion criteria were: (i) history of significant alcohol consumption; (ii) background of any known important acute or chronic pathological conditions such liver and/or renal failure, immunological disorders, VIH, cancer, among others); (iii) unlikely to cooperate with the study regime. During the study 8 subjects were voluntary retired and 3 additional were excluded by have the insulinaemia over normal range (> 100 µU /mL).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Propolis diversity use in human health 6 months case-control, randomized, double blind, placebo controlled | — |
Secondary
| Measure | Time frame |
|---|---|
| Propolis in human health 6 months case-control, randomized, double blind, placebo controlled | — |
Countries
Chile
Contacts
Public ContactElba Leiva
Universidad de Talca
Outcome results
None listed