Expired Study
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Dallas, Texas 75230


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.

Study summary:

Participants will be randomized to either a control or treatment group taking the dietary supplement containing a soy lecithin-derived N-oleoyl-phosphatidyl-ethanolamine (NOPE) and caffeine free Green Tea-derived epigallocathchin gallate (EGCG) whose trade name is PhosphoLean. The outcome is to determine the effects on indices of weight loss and appetite suppression. Participants will return at 6, 12, and 16 weeks for clinical measures.


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 have or history of cancer, heart disease, anemia, diabetes, depression



Primary Contact:

Principal Investigator
Conrad Earnest, PhD
The Cooper Institute

Backup Contact:


Location Contact:

Dallas, Texas 75230
United States

There is no listed contact information for this specific location.

Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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