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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00529919
Other study ID # F050124003
Secondary ID
Status Completed
Phase N/A
First received September 12, 2007
Last updated September 12, 2007
Start date March 2005
Est. completion date June 2007

Study information

Verified date September 2007
Source University of Alabama at Birmingham
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The primary aim of this research project is to determine whether the incorporation of food products containing medium chain triglyceride (MCT) oil in a weight-loss program results in a different degree of weight-loss and total and regional fat mass loss than the incorporation of extra light olive oil. The secondary goals are to test whether there are differences in in metabolic risk profile changes between the 2 diets. We hypothesize that men and women who consumed MCT oil as part of their weight loss program will lose more weight and body fat than those who consume olive oil in their weight loss diet.


Recruitment information / eligibility

Status Completed
Enrollment 53
Est. completion date June 2007
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 19 Years to 50 Years
Eligibility Inclusion Criteria:

- body mass index 27-33 kg/m2

- pre-menopausal women

- weight stable for at least 6 months

- normal score on Brief Symptoms Inventory questionnaire

Exclusion Criteria:

- chronic disease

- weight loss treatment

- medication known to affect body weight

- unstable blood pressure, glucose, lipid levels

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Weight loss
Weight loss study including consumption of either 22-25 g of medium chain triglyceride oil or olive oil

Locations

Country Name City State
United States University of Alabama at Birmingham Birmingham Alabama

Sponsors (2)

Lead Sponsor Collaborator
University of Alabama at Birmingham International Life Sciences Institute

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in body weight and fat mass, change in plasma lipid concentrations, fasting glucose and fasting insulin 16 weeks
Secondary Change in blood pressure, change in fat-free mass 16 weeks
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