Actively Recruiting
Comparative Evaluation of Probiotic-Based Versus Ethyl Lauroyl Arginate-Containing Mouthwashes on Streptococcus Mutans Counts, Dental Plaque Accumulation, and Salivary pH in a Group of Egyptian School Children: A Randomized Controlled Clinical Trial
Led by Al-Azhar University · Updated on 2026-01-21
66
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to compare the effectiveness of probiotic-based mouthwashes and ethyl lauroyl arginate-containing mouthwashes in reducing the amount of Streptococcus mutans bacteria, dental plaque buildup, and changes in saliva pH among Egyptian schoolchildren aged 6 to 12 years. Dental caries is a common chronic infectious disease in this population, with S. mutans playing a key role in enamel damage and plaque formation. Ethyl lauroyl arginate is known for its strong antibacterial effects and ability to reduce biofilm while preserving the balance of the oral microbiome. Participants will be randomly assigned to one of three groups: one group will use a probiotic mouthwash by rinsing 5 ml twice daily for 30 seconds over 28 days; a second group will use an ethyl lauroyl arginate mouthwash with the same dosing and duration; the third group will receive professional dental cleaning (scaling and polishing) at the start and then use only regular toothpaste twice daily without any additional mouthwash for 28 days. During the study, children will be monitored for changes in S. mutans levels, dental plaque accumulation, and salivary pH after 28 days of treatment. Researchers will measure these outcomes to evaluate how each treatment affects oral health. The trial includes baseline professional cleaning for one group, and all participants will be followed for the full 28-day period to assess the impact of the interventions on their oral bacteria and plaque levels.
CONDITIONS
Brief Title
Probiotic-Based Versus Ethyl Lauroyl Arginate-Containing Mouthwashes on Streptococcus Mutans Counts, Dental Plaque Accumulation, and Salivary pH in a Group of Egyptian School Children
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Healthy Egyptian schoolchildren aged 6-12 years
- Good general health
- Mild to moderate dental plaque accumulation
- Parental or caregiver willingness to provide consent
You will not qualify if you...
- Antibiotic or antimicrobial use within the last month
- Allergies to the mouthwash components
- Systemic diseases affecting oral health
- Orthodontic appliances or extensive dental restorations
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 28 days
Participants use assigned mouthwash or receive professional dental cleaning to manage dental plaque and bacteria.
Daily mouthwash use twice daily or 1 baseline professional cleaning visit depending on group
Trial Site Locations
Total: 1 location
1
Al-Azhar University (Faculty of Dentistry)
Cairo, Egypt, 11651
Actively Recruiting
Research Team
M
Mohamed O Abdelrazik, MBBCH
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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