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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | LC-Plasma | 1 tablet containing 50mg LC-Plasma is taken daily for 4 weeks |
| OTHER | Placebo | 1 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.