Clinical Trials Directory

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UnknownNCT04124276

Evaluation of Efficacy of Lycium Barbarum Polysaccharide in Patients With Major Depressive Disorder

Evaluation of Efficacy of Lycium Barbarum Polysaccharide in Patients With Major Depressive Disorder: a Randomized,Placebo-controled Trial

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
284 (estimated)
Sponsor
Guangzhou Psychiatric Hospital · Other Government
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

Lycium barbarum, a traditional Chinese herbal medicine, is a commonly used herb in the traditional Chinese pharmacopoeia. Its main active ingredient, lycium barbarum polysaccharide (LBP), is reported to have neuroprotective effects. Animal studies suggested that LBP has neuroprotective effect on optic ganglion cells. In animal models of depression, LBP can improve depressive symptom by improving synaptic plasticity. However, its clinical effect remains to be studied. We will conduct a 6-week double-blind, randomized, placebo-con-trolled trial in patients with major depressive disorder (MDD). The purpose of this clinical trial is to investigate the efficacy of LBP in patients with MDD.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTLycium barbarum polysaccharideExperimental groups take Lycium barbarum polysaccharide (LBP) (300mg/day) for 6 weeks
DIETARY_SUPPLEMENTPlaceboPlacebo control group takes placebo (300mg/day) for 6 weeks.

Timeline

Start date
2019-11-01
Primary completion
2020-12-30
Completion
2021-06-01
First posted
2019-10-11
Last updated
2020-10-30

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04124276. Inclusion in this directory is not an endorsement.