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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01581697
Other study ID # up 4100/07
Secondary ID
Status Recruiting
Phase Phase 1/Phase 2
First received April 17, 2012
Last updated April 19, 2012

Study information

Verified date April 2012
Source Instituto de Cardiologia do Rio Grande do Sul
Contact Lúcia Campos Pellanda, Doctor
Phone +55 51 32303600
Email lupellanda@uol.com.br
Is FDA regulated No
Health authority Brazil: Ministry of Health
Study type Interventional

Clinical Trial Summary

Atherosclerosis is the leading cause of death and disability in adults. However, investigations suggest that the basic pathology of heart disease as more severe myocardial infarction which usually reach mainly middle-aged or above, starts from childhood. Hypercholesterolemia is one of the most important risk factors for atherosclerosis in adults and children, is associated with early deposition of lipids in the aorta and coronary arteries.

Among other recommendations for prevention and treatment of heart disease and risk factors, is the recommendation to encourage the intake of soluble fiber. The oats, a major source of soluble fiber, has been recognized as a potential component of the diet to lower blood cholesterol levels, this effect is attributed mainly to the beta-glucan, a type of soluble fiber present in large quantities in oats. In 1997 the Food and Drug Administration admitted that the oat bran, oat flakes and oatmeal may have beneficial effects for health with the recommendation of daily intake of 3g of beta-glucan from oats and a food that brings a claim for promotion health, must provide, without enrichment, at least 1 gram of beta-glucan per serving.

The objective of this project will be compared by randomized clinical trial, the impact of intake of oats, for 8 weeks in the lipid profile of children and adolescents with dyslipidemia.

Will be included in the study 120 volunteers aged between 5 and 16 years who are in nutritional monitoring for at least 1 month. The subjects will be randomly divided into 2 groups, with a control group and another intervention will receive 3 tablespoons of soup filled with oat bran, which corresponds to 3g of beta-glucan, along with breakfast, lunch and dinner. Patients will be monitored with consultations on the 2nd, 4th and 8th weeks of treatment. Blood sample will be performed, to obtain the lipid profile of patients, at the beginning and end of the study. To compare the groups are used Student's t and squared chi. The alpha of 0.05 is considered critical. The program will be used Statistical Package for the Social Sciences (SPSS) version 15.0.

It is expected a decrease in serum levels of total cholesterol and LDL-c. Thus, living habits and healthy alternatives to prevent these risk factors should be done since childhood, especially in children who already have cholesterol levels of change.


Recruitment information / eligibility

Status Recruiting
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 5 Years to 16 Years
Eligibility Inclusion Criteria:

- Male/Female

- Age limits 5 years-16 years

Study Design

N/A


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Oat bran


Locations

Country Name City State
Brazil Instituto de Cardiologia do Rio Grande do Sul - Fundação Universitária de Cardiologia Porto Alegre Rio Grande do Sul

Sponsors (3)

Lead Sponsor Collaborator
Instituto de Cardiologia do Rio Grande do Sul CNPq Universal, Quaker Oats Company

Country where clinical trial is conducted

Brazil, 

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