Clinical Trials Directory

Trials / Completed

CompletedNCT01416051

Efficacy of Olibra: A 12 Week Controlled Trial

Efficacy of Olibra: A 12 Week Randomized Controlled Trial, and Review of Prior Studies

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
82 (actual)
Sponsor
Pennington Biomedical Research Center · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Accepted

Summary

Today's obesogenic environment, favors behavioral choices that lead to an excess of energy intake over expenditure, and consequently weight gain. Intervention strategies that harness the body's own appetite and satiety regulating signals could provide an effective means of countering excessive energy intake. The purpose of this study was to investigate whether a vegetable oil emulsion (Olibra) would result in weight loss that was associated with a reduction in food intake.

Detailed description

71 healthy subjects were enrolled (60 females, 11 males; Age: 18 - 60 years, BMI 25 - 40 kg/m2) in a two-phased, randomized, placebo-controlled, double-blind, parallel trial. During a 12-week period, Olibra was compared with a placebo (milk fat). Food intake testing was conducted on three days and anthropometric data was collected on 7 days. Key outcome measures were, body weight, body composition, energy intake, and appetite ratings.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTOlibraFractionated palm oil and fractionated oat oil in the proportion of 95:5
OTHERPlacebo100% milk fat

Timeline

Start date
2005-01-01
Primary completion
2006-11-01
Completion
2006-11-01
First posted
2011-08-12
Last updated
2015-12-18

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01416051. Inclusion in this directory is not an endorsement.