Status:
COMPLETED
A Clinical Study Conducted in the Bangkok, Thailand Area, to Investigate the Clinical Efficacy of a New Toothpaste
Lead Sponsor:
Colgate Palmolive
Conditions:
Oral Malodor
Eligibility:
All Genders
18-70 years
Phase:
PHASE3
Brief Summary
To investigate the clinical efficacy of a new toothpaste containing 0.454% stannous fluoride as compared to a regular fluoride toothpaste containing 0.76% sodium monofluorophosphate on oral malodor re...
Eligibility Criteria
Inclusion
- Male and female adults between the ages of 18-70 (inclusive)
- Subjects must be in general good health
- Subjects must be in good oral health based on self-assessment
- Subjects must be available for the duration of the study for all time point assessments
- Subjects were required to possess a minimum of 20 natural uncrowned teeth (excluding third molars)
- Subjects were required to sign an Informed Consent form
- No known history or allergies to personal care/consumer products or their ingredients.
Exclusion
- Participated in any other oral clinical studies during the duration of this study
- Had full or partial (upper or lower) dentures
- Women who are pregnant or lactating (breast feeding)
- Use of tobacco products, (5) History of allergies to common mouthwash ingredients
- Use of phenolic flavored products, such as mint flavored candies and chewing gum the morning of the study of during the sampling periods
- Immune compromised individuals (HIV, AIDS, immune suppressive drug therapy
- Individuals who, due to medical conditions cannot go without eating or drinking for the post use treatment evaluation time points (6-hours plus overnight).
Key Trial Info
Start Date :
December 21 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 12 2018
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT07223073
Start Date
December 21 2017
End Date
January 12 2018
Last Update
October 31 2025
Active Locations (1)
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1
M U International Oral Science Research, Ltd.
Bangkok, Bangkok, Thailand, 10250