Hypertriglyceridemia
Conditions
Interventions
Analytical, observational, descriptive cohort study with prospective temporality. Men (300 participants) and women (300 participants) enrolled in the study will receive a high-fat test meal containing
G07.203.300.375
Sponsors
Universidade Federal Fluminense - Instituto de Saúde de Nova Friburgo
Sociedade União Beneficente Humanitária dos Operários
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Residing in the mountainous region of the state of Rio de Janeiro; Attend the Sociedade Beneficente Humanitaria dos Operarios; Men; Women; Over 18 years
Exclusion criteria
Exclusion criteria: Who do not adhere to the experimental protocol or do not attend one of the planned visits; who use lipid lowering drugs; carriers of genetic disorders that affect lipid metabolism; who are on an energy restricted diet or some macronutrient at the time of the study or in the last two months prior to the study; strict vegetarians, lactovegetarians and ovolactovegetarians; who regularly consume two or more doses of alcoholic beverages 5 grams of alcohol; under 18 years old; mentally disabled
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Found Outcome 1: Four hours after eating the test meal, blood triglycerides assessed by biochemical assay raised above 20 percent;Expected outcome 1: Four hours after eating the test meal, blood triglycerides assessed by biochemical assay are expected to rise by at least 20 percent | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes are expected | — |
Countries
Brazil
Contacts
Public ContactCaroline Bottino
Universidade Federal Fluminense - Instituto de Saúde de Nova Friburgo
Outcome results
None listed