Overview
A Clinical Study to Assess the Gingivitis Effects of Various Dentifrices
Status:
Completed
Completed
Trial end date:
2022-02-06
2022-02-06
Target enrollment:
0
0
Participant gender:
All
All
Summary
The objective of this learning clinical study is to assess the gingivitis effects of four different dentifrices over a 3-month period.Phase:
N/AAccepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Procter and GambleTreatments:
Fluorides
Fluorophosphate
Tin Fluorides
Criteria
Inclusion Criteria:- Be at least 18 years of age;
- Provide written informed consent prior to participation and be given a signed copy of
the informed consent form;
- Be in general good health as determined by the Investigator based on a review of the
health history/update for participation in the trial;
- Have at least 16 gradable teeth;
- Have mild to moderate gingivitis with a range of 10% to 70% bleeding sites;
- Agree to return for scheduled visits and follow the study procedures;
- Agree to refrain from use of any non-study oral hygiene products for the duration of
the study;
- Agree to delay any elective dentistry, including dental prophylaxis, until the
completion of the study.
Exclusion Criteria:
- Having taken antibiotic, anti-inflammatory, or anti-coagulant medications within 4
weeks of the Baseline Visit;
- Have any oral conditions that could interfere with study compliance and/or examination
procedures, such as widespread caries, soft or hard tissue tumor of the oral cavity,
or advanced periodontal disease;
- Removable oral appliances;
- Fixed facial or lingual orthodontic appliances;
- Self-reported pregnancy or lactation;
- Any diseases or condition that might interfere with the safe participation in the
study; and
- Inability to undergo study procedures.