Clinical Trials Directory

Trials / Completed

CompletedNCT01046968

Lepticore in Metabolic Syndrome and Weight Loss

The Use of LeptiCore® in Reducing Fat Gain and Managing Weight Loss in Patients With Metabolic Syndrome

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
92 (actual)
Sponsor
University of Yaounde 1 · Academic / Other
Sex
All
Age
19 Years – 52 Years
Healthy volunteers
Accepted

Summary

Metabolic syndrome is directly related to obesity. This study investigated the use of a plant based formulation to improve on the condition of people with metabolic syndrome.

Detailed description

LeptiCore is a proprietary combination of various ingredients which have been shown to have properties which could be beneficial to weight loss in obese and overweight human subjects. This study evaluates the effect of Lepticore on bodyweight as well as parameters associated with obesity and metabolic syndrome. The study was an 8 week randomized, double-blind, placebo-controlled design involving 92 obese (mean BMI\>30kg/m2) participants (37 males; 55 females; ages 19-52; mean age = 30.7). The participants were randomly divided into three groups: placebo (n=30), LeptiCore formula A (low dose) (n=31) and LeptiCore formula B (high dose) (n=31). Capsules containing the placebo or active formulations were administered twice daily before meals with 300 ml of water. None of the participants followed any specific diet nor took any weight-reducing medications for the duration of the study. A total of 12 anthropomorphic and serological measurements were taken at the beginning of the study and after 2, 4, 6, and 8 weeks of treatment.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTLepticore300 mg twice daily

Timeline

Start date
2009-08-01
Primary completion
2009-11-01
Completion
2009-11-01
First posted
2010-01-12
Last updated
2010-01-12

Locations

1 site across 1 country: Cameroon

Source: ClinicalTrials.gov record NCT01046968. Inclusion in this directory is not an endorsement.