Clinical Trials Directory

Trials / Completed

CompletedNCT06837961

LC-Plasma on Immune Response and Reducing Symptoms of Upper Respiratory Infectious Diseases

The Effects of Lactococcus Lactis JCM 5805 (LC-Plasma) Lactic Acid Bacteria on Immune Response and Reducing Symptoms of Upper Respiratory Infectious Disease in Australian Healthy Adults. Randomized Placebo-controlled Double-blind Parallel Group Study.

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
241 (actual)
Sponsor
RDC Clinical Pty Ltd · Industry
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Accepted

Summary

The goal of this study is to evaluate the effects of LC-Plasma on the innate and acquired immune systems, including the activation of pDCs, which play a role in virus elimination, as well as to assess its efficacy in reducing clinical symptoms of upper respiratory infectious diseases in healthy adults. Researchers will compare LC-Plasma to placebo, participants will take a tablet containing LC-Plasma or placebo daily for 4 weeks.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTLC-Plasma1 tablet containing 50mg LC-Plasma is taken daily for 4 weeks
OTHERPlacebo1 tablet containing 50mg MCC is taken daily for 4 weeks

Timeline

Start date
2025-04-29
Primary completion
2025-11-03
Completion
2025-11-03
First posted
2025-02-20
Last updated
2025-11-18

Locations

1 site across 1 country: Australia

Source: ClinicalTrials.gov record NCT06837961. Inclusion in this directory is not an endorsement.