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To check the effectiveness of probiotic toothpaste in reducing caries causing bacteria in the saliva.

Effect of probiotic toothpaste on Streptococcus Mutans and Lactobacillus in saliva-A randomized control trial - NIL

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072664
Enrollment
60
Registered
2024-08-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K029- Dental caries, unspecified

Interventions

Intervention1: probiotic toothpaste: Purexa Probiotic Toothpaste to be used twice daily for brushing teeth for 30 days. Control Intervention1: Regular toothpaste: Any regular toothpaste without probi

Sponsors

Dr Twinkle Sharma
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age between 18 to 25 years. 2.Participants with all fully erupted teeth. 3.Participants with inactive caries. 4.No underlying systemic condition. 5.Habit of brushing twice daily.

Exclusion criteria

Exclusion criteria: 1.Enrolled in any other clinical trial 30 days prior to randomization. 2.With major dental conditions such as periodontal disease, dental caries and/or xerostomia or systemic diseases which could directly or indirectly affect plaque formation. 3.Using any antimicrobial mouth rinses, probiotics (unrelated to the study) antibiotics or anti-inflammatories medications within one month prior to and during the study. 4.With allergies to any ingredient present in the lorodent probiotic complex. 5.Experiencing any nausea, fever, vomiting, bloody diarrhea or severe abdominal pain within the 30 days prior to commencing the study. 6. Those who were immunocompromised and/or had a major underlying medical condition or ENT problem. 7.Had recent (within the past 45 days) or planned (within the past 90 days) surgery of any kind. 8.With a history of smoking or alcohol consumption. 9.Pregnant and lactating females. 10. Who were unable to make informed consent.

Design outcomes

Primary

MeasureTime frame
1.Levels of streptococcus mutans in saliva. 2.Levels of lactobacillus in saliva.Timepoint: 1.Levels of streptococcus mutans and lactobacillus in saliva at baseline 2.Levels of streptoccus mutans and lactobacillus in saliva after one month

Secondary

MeasureTime frame
1.Change in levels of Streptococcus mutans and Lactobacillus in saliva after one month of probiotic toothpaste use.Timepoint: 1.Baseline (Day 0): Initial saliva sample collection before the start of the intervention to determine the baseline levels of Streptococcus mutans and Lactobacillus. 2.After 30 Days (Day 30): Follow-up saliva sample collection at the end of the 30-day intervention period to measure the levels of Streptococcus mutans and Lactobacillus and determine the change from baseline.

Countries

India

Contacts

Public ContactDr Preety Gupta

Swami Devi Dyal Hospital and Dental College

dr.preety86@gmail.com9876441194

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026