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Clinical Trial Summary

The objective of the study is to compare the effect of a 6-week supplementation with a dietary supplement based on plant extracts to the effect of placebo, in patients with a moderate depressive episode (F32.1 by ICD10 definition) and with moderate symptoms (score HAM-D ≥ 16 and ≤ 23).


Clinical Trial Description

Longitudinal, comparative, randomized, placebo-controlled interventional study in 2 parallel groups, double-blind, monocentre, aimed at demonstrating the superiority of the combination of plants over placebo on depressive symptoms. Each patient will be followed for a maximum of 6 weeks, with 3 visits to the doctor. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05199545
Study type Interventional
Source Larena SAS
Contact Samira Aït Abdellah
Phone (0)1 45 51 78 77
Email s.aitabdellah@pileje.com
Status Recruiting
Phase N/A
Start date April 26, 2022
Completion date May 1, 2024

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