Probiotic Toothpaste to Assess Microbial Colonization

Sponsor
BLIS Technologies Limited (Industry)
Overall Status
Not yet recruiting
CT.gov ID
NCT06015958
Collaborator
(none)
20
1
2
4.9
4.1

Study Details

Study Description

Brief Summary

The aim of this study is to evaluate the colonization efficacy of probiotic toothpastes in healthy adults

Condition or Disease Intervention/Treatment Phase
  • Other: Streptococcus salivarius M18 toothpaste (1 million cfu)
  • Other: Streptococcus salivarius M18 toothpaste (10 million cfu)
N/A

Detailed Description

This is a double blind randomized controlled study with no cross over to evaluate the colonization efficacy of toothpaste containing a commercially available probiotic bacterium Streptococcus salivarius M18.

Participants will be randomly assigned to one of 2 groups for brushing teeth with a probiotic toothpaste containing two different doses of Streptococcus salivarius M18 over a seven day period. Saliva samples will be collected at predetermined time points pre and post intervention. Colonization efficacy will be determined by enumerating the probiotic in the saliva samples using standard microbiological techniques.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Participants will be randomly assigned to one of the 2 groups for brushing teeth with a probiotic toothpaste containing different doses of Streptococcus salivarius M18 Study Group A: BLIS M18 Toothpaste (10 million Cfu/dose) (n = 10) Study Group B: BLIS M18 Toothpaste (1 Million Cfu/dose) (n = 10)Participants will be randomly assigned to one of the 2 groups for brushing teeth with a probiotic toothpaste containing different doses of Streptococcus salivarius M18 Study Group A: BLIS M18 Toothpaste (10 million Cfu/dose) (n = 10) Study Group B: BLIS M18 Toothpaste (1 Million Cfu/dose) (n = 10)
Masking:
Single (Participant)
Masking Description:
A staff member not part of the study group will be assigned to distribute blinded samples. The participant or the investigators will not be aware of the dose groups.
Primary Purpose:
Basic Science
Official Title:
Colonisation Efficacy of Streptococcus Salivarius M18 Toothpaste
Anticipated Study Start Date :
Oct 1, 2023
Anticipated Primary Completion Date :
Nov 29, 2023
Anticipated Study Completion Date :
Feb 28, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Active Comparator: Streptococcus salivarius M18 toothpaste dose 1

Streptococcus salivarius M18 toothpaste containing 1 million cfu/g

Other: Streptococcus salivarius M18 toothpaste (1 million cfu)
Probiotics Streptococcus salivarius M18 toothpaste 1 million cfu/g In this study, a toothpaste formulation containing S. salivarius M18 will be evaluated for its potential for delivering the probiotic to the oral cavity.

Active Comparator: Active Comparator: Streptococcus salivarius M18 toothpaste dose 2

Streptococcus salivarius M18 toothpaste containing 10 million cfu/g

Other: Streptococcus salivarius M18 toothpaste (10 million cfu)
Probiotics Streptococcus salivarius M18 toothpaste 10 million cfu/g In this study, a toothpaste formulation containing S. salivarius M18 will be evaluated for its potential for delivering the probiotic to the oral cavity.

Outcome Measures

Primary Outcome Measures

  1. Change in Microbial colonization from baseline (Day 0) to 1 hour [1 hour post intervention]

    Study will determine the change in the microbial colonization efficacy of two different doses of S. salivarius M18 in a toothpaste format. Study will determine the change in microbial colonization efficacy of Streptococcus salivarius M18 in a toothpaste format. The saliva Statistical analysis (e.g. ANOVA) will be carried out to compare the participants data from baseline to one hour after later across three different formulations with the level of significance of p≤0.05.Overall colonization based on percentage of population colonized for different interventions will also be analyzed average and standard deviation functions using appropriate statistical analysis software (e.g. Microsoft Excel, GraphPad Prism).

  2. Change in Microbial colonization from baseline (Day 0) to 8 hours [8 hours post intervention]

    Study will determine the change in the microbial colonization efficacy of three different doses of S. salivarius M18 in a toothpaste format. Study will determine the change in microbial colonization efficacy of Streptococcus salivarius M18 in a toothpaste format. The saliva Statistical analysis (e.g. ANOVA) will be carried out to compare the participants data from baseline to one hour after later across three different formulations with the level of significance of p≤0.05.Overall colonization based on percentage of population colonized for different interventions will also be analyzed average and standard deviation functions using appropriate statistical analysis software (e.g. Microsoft Excel, GraphPad Prism).

  3. Change in Microbial colonization from baseline (Day 0) to 24 hours [24 hours post intervention]

    Study will determine the change in the microbial colonization efficacy of three different doses of S. salivarius M18 in a toothpaste format. Study will determine the change in microbial colonization efficacy of Streptococcus salivarius M18 in a toothpaste format. The saliva Statistical analysis (e.g. ANOVA) will be carried out to compare the participants data from baseline to one hour after later across two different formulations with the level of significance of p≤0.05.Overall colonization based on percentage of population colonized for different interventions will also be analyzed average and standard deviation functions using appropriate statistical analysis software (e.g. Microsoft Excel, GraphPad Prism).

  4. Change in Microbial colonization from baseline (Day 0) to 8 hours post last dose [8 hours after last dose following 7 days of daily brushing with probiotic toothpaste.]

    Study will determine the change in the microbial colonization efficacy of two different doses of S. salivarius M18 in a toothpaste format. Study will determine the change in microbial colonization efficacy of Streptococcus salivarius M18 in a toothpaste format. The saliva Statistical analysis (e.g. ANOVA) will be carried out to compare the participants data from baseline to one hour after later across three different formulations with the level of significance of p≤0.05.Overall colonization based on percentage of population colonized for different interventions will also be analyzed average and standard deviation functions using appropriate statistical analysis software (e.g. Microsoft Excel, GraphPad Prism).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • In general good health

  • Practise good oral hygiene

Exclusion Criteria:-

  • Have a history of autoimmune disease or are immunocompromised.

  • Are on concurrent antibiotic therapy or regular antibiotic use within last 1 week

  • History of allergy (e.g. dairy).

Contacts and Locations

Locations

Site City State Country Postal Code
1 Blis Technologies Ltd Dunedin Otago New Zealand 9012

Sponsors and Collaborators

  • BLIS Technologies Limited

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
BLIS Technologies Limited
ClinicalTrials.gov Identifier:
NCT06015958
Other Study ID Numbers:
  • BLTCT2022/9
First Posted:
Aug 29, 2023
Last Update Posted:
Aug 29, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by BLIS Technologies Limited
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 29, 2023