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Efficacy Study in Phytotherapy of an Association of Plants in the Improvement of Psychological Well-being

NCT05199545 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 126

Last updated 2025-07-15

No results posted yet for this study

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).

Conditions

  • Psychological Well-being

Interventions

DIETARY_SUPPLEMENT

Dietary supplement

Dietary supplement under study is based on Rhodiola rosea L. and Crocus sativus L. extracts

OTHER

Placebo

Placebo of the dietary supplement

Sponsors & Collaborators

  • Université Catholique de Louvain

    collaborator OTHER

  • Larena SAS

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-04-26
Primary Completion
2024-05-07
Completion
2024-05-07

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05199545 on ClinicalTrials.gov