Effects of periodic ingestion of Lactobacillus plantarum on human oral pathogens
Not Applicable
Completed
- Conditions
- Not Applicable
- Registration Number
- KCT0003996
- Lead Sponsor
- Seoul National University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Those who have decided to voluntarily participate in this study and have agreed in writing to the subject agreement.
- Those who can understand and follow the instructions, and participate in the entire period of the study.
Exclusion Criteria
- Those who have severely impaired renal function or liver function.
- Those who are currently on medication to treat other diseases.
- Those who have side-effects such as abdominal pain and diarrhea when taking lactobacillus or Probiotics.
- Those who have participated in other clinical trials within 3 months (90 days) before participating in this study.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The number of Escherichia coli and Staphylococcus aureus in oral cavity before consumption of Lactobacillus plantarum
- Secondary Outcome Measures
Name Time Method The number of Escherichia coli and Staphylococcus aureus in oral cavity after consumption of Lactobacillus plantarum