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Clinical Trial Summary

Evaluation of the efficacy of Phaseolus vulgaris L. dry extract on weight modulation.


Clinical Trial Description

Monocentric, prospective, randomized, single-blind clinical trial to evaluate the effects of Phaseolus vulgaris L. dry extract (test) on weight reduction and on metabolic parameters after 12 weeks of supplementation. The efficacy on weight reduction will be evaluated in comparison with the placebo group (control). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06193577
Study type Interventional
Source IBSA Farmaceutici Italia Srl
Contact Carmelo Gusmano, MD
Phone +393891136444
Email carmelo.gusmano@yahoo.it
Status Recruiting
Phase N/A
Start date November 8, 2023
Completion date April 30, 2025

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