N/A
N=87
A Four-Week Study to Measure the Effectiveness of an Experimental Mouthwash Used After Teeth Cleaning
Dental Plaque
Bottom Line
View on ClinicalTrials.gov: NCT01462110 ↗Enrolled (actual)
87
Serious AEs
1.2%
Results posted
Mar 2020
Primary outcome: Primary: Whole-mouth Mean Modified Gingival Index (MGI) — 2.199; 1.948 Units on a scale — p=<0.001
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- 19416-154-1 (Device); W002194-0221P (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Johnson & Johnson Consumer and Personal Products Worldwide
- Primary completion
- Dec 2011
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Whole-mouth Mean Modified Gingival Index (MGI) |
2.189; 2.067 | <0.001 sig |
| PRIMARY Whole-mouth Mean Plaque Index (PI) |
2.880; 1.987 | <0.001 sig |
| SECONDARY Whole-mouth Mean Modified Gingival Index (MGI) |
2.189; 2.067 | <0.001 sig |
| SECONDARY Whole-mouth Mean Plaque Index (PI) |
2.880; 1.987 | <0.001 sig |
| SECONDARY Whole-mouth Mean Bleeding Index (BI) |
0.120; 0.057 | <0.001 sig |
| SECONDARY Whole-mouth Mean Bleeding Index (BI) |
0.120; 0.057 | <0.001 sig |
| SECONDARY Microbiological Assessments - Absolute Counts |
1.868; 1.847; 0.910; 0.663; 1.050; 1.018 | — |
| SECONDARY Microbiological Assessments - LOG Counts |
5.089; 5.154; 4.721; 4.617; 4.882; 4.915 | — |
Summary
This study will test the idea that using an experimental mouth rinse after each time you brush your teeth will result in a healthier mouth than using the regular mouth rinse. Participants will be expected to avoid oral hygiene (like brushing teeth or using mouthwash) for at least 12 hours before each visit and will not be allowed to eat, drink or smoke for at least 4 hours before each visit.
At the first visit, the study will be explained to you in detail and you will be allowed to ask any questions you may have before signing a consent form. You will complete a medical/dental history and the dentist will examine your mouth, during which he will poke your gums and scrape some plaque off your teeth for testing. If you do not meet the requirements to continue in the trial, you will be told that you do not need to return for more testing.
If you meet requirements to continue, you will have an equal chance of being assigned to use either of the two mouth rinses being studied. You will be given a diary, toothbrush, toothpaste, and your assigned mouth rinse, with instructions on how they must be used.
You will be instructed not to use any unassigned oral care products and to follow your usual eating habits. You will be given appointments to return two times within the next four weeks. At those visits, the staff will check to make sure you're following the instructions and ask how you're feeling, and the dentist will do the same thing he did during the first visit.
Eligibility Criteria
Inclusion Criteria
- Males and females at least 18 years of age and in good general health.
- Must display adequate oral hygiene (i.e., brush teeth daily and exhibit no signs of oral neglect).
- Volunteers must read, sign, and receive a copy of the Informed Consent Form after the nature of the study has been fully explained.
- Must be willing to use the products according to instructions and be available for appointments.
- Baseline dental measurements meet protocol-specified criteria.
- Willingness to refrain from using all oral hygiene procedures within 12-18 hours prior to each visit.
- Refrain from eating, drinking or smoking for four hours prior to each visit.
Exclusion Criteria
- Lip, tongue, or other form of oral piercing.
- Fixed or removable orthodontic appliance (such as bridges, braces or dentures).
- Pregnancy or breast-feeding at any time during the trial.
- Any medical, dental or psychiatric condition, abnormality or history, or use of any product or drug, that (per protocol or in the opinion of the investigator) may increase the risk to the subject associated with trial participation or investigational product administration, or interfere with the interpretation of trial results.
Data sourced from ClinicalTrials.gov (NCT01462110). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.