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Clinical Trial Summary

The purpose of the study is to describe, over 6 weeks, the evolution of depressive symptoms in patients with mild to moderate major depression in a strategy with Phytostandard® Rhodiola-Saffron supplementation


Clinical Trial Description

For this study, 52 patients are going to be included. They will have a supplementation of Phytostandard® rhodiola/saffron, from 2 tablets per day during 42 days.

on the one hand, during the two visits (inclusion and follow-up), the investigator completes the Hamilton Depression Scale (HAM-D) and the Clinical Global Impression (CGI). During the inclusion visit, he completes with his patient CIM-10 for depression diagnostic.

on the other hand, patients complete HAD 4 times : just after the inclusion visit, at day 14, at day 28 and just before the follow-up visit. He completes the Patient Global Impression too at each time. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02981225
Study type Observational
Source Pileje
Contact
Status Completed
Phase
Start date November 8, 2016
Completion date May 31, 2017

See also
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Completed NCT03238872 - Trial of Prompt Mental Health Care N/A
Recruiting NCT06430476 - EMI Therapy for Depression in Hong Kong N/A