Meta-analysis of Stannous Fluoride and the Effects on Dental Plaque
A Review of Meta-Analyses on Bioavailable Stannous Fluoride Dentifrices: Effects on Dental Plaque
1 other identifier
observational
2,359
1 country
1
Brief Summary
The aim of this 18 study analysis was to compare the effect of bioavailable stannous fluoride (SnF2) dentifrices when used up to 3 months on dental plaque relative to a positive or negative control dentifrice.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2018
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 8, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 30, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
November 30, 2018
CompletedFirst Submitted
Initial submission to the registry
July 1, 2019
CompletedFirst Posted
Study publicly available on registry
July 5, 2019
CompletedNovember 18, 2023
November 1, 2023
11 months
July 1, 2019
November 14, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
Dental Plaque Scores
Change from baseline as measured by mean plaque score reduction from baseline (via Quigley-Hein, Turesky Modification Index or Rustogi Modification of the Navy Plaque index).
Up to 12 weeks
Study Arms (3)
Stannous Fluoride Dentifrice
Twice daily brushing
Positive control dentifrice
Twice daily brushing
Negative control dentifrice
Twice daily brushing
Interventions
Positive control dentifrice containing (0.3%) triclosan.
Negative control dentifrice containing either sodium fluoride (0.243%) or sodium monofluorophosphate (0.76%)
Eligibility Criteria
This meta-analysis includes healthy adult male and females.
Contact the study team to discuss eligibility requirements. They can help determine if this study is right for you.
Sponsors & Collaborators
Study Sites (1)
Multiple P&G Investigation Clinical Sites
Cincinnati, Ohio, 45040, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 1, 2019
First Posted
July 5, 2019
Study Start
January 8, 2018
Primary Completion
November 30, 2018
Study Completion
November 30, 2018
Last Updated
November 18, 2023
Record last verified: 2023-11