LEAN Project: Weight Loss and Appetite Suppression

The primary aim is to examine whether the intake of PhosphoLEAN is effective in aiding a cohort of women in losing weight. Participants taking the supplement will have significantly greater improvement in study outcomes than those taking the placebo.

Official Title

The Effect of Soy Lecithin-Derived N-Oleoyl-Phosphatidyl-Ethanolamine (NOPE) and Green Tea-Derived Epigallocatechin Gallate (EGCG) on Indices of Weight Loss and Appetite Suppression

Conditions

• Weight Loss

Study Type

Interventional

Study Design

Treatment, Randomised, Double-Blind, Placebo Control, Single Group Assignment, Safety/Efficacy Study

Further Details

Primary Outcome Measures:

• Weight Loss
• Appetite Suppression

Study Start

April 2005

Eligibility & Criteria

Eligibility

• Ages Eligible for Study: 30 years to 45 years
• Genders Eligible for Study: Female
• Accepts Healthy Volunteers: Yes

Criteria

Inclusion Criteria:

• 30-45 years, women, overweight or obese class I, premenopausal, maintain current diet and exercise regimen

Exclusion Criteria:

• Pregnant or planning to become pregnant
• Currently has or history of
  • Cancer
  • Heart disease
  • Anaemia
  • Diabetes
  • Depression

Total Enrolment

60

Contact Details

Please refer to this study by its ClinicalTrials.gov identifier: NCT00153790

Locations

The Cooper Institute      
Dallas, Texas, United States, 75230

Sponsors and Collaborators

The Cooper Institute

Chemi Nutra

Investigators

Principal Investigator:

Conrad Earnest, PhD 
The Cooper Institute