Gingivitis
Conditions
Keywords
gingivitis index, plaque index, discoloration index, mouth rinse, amine fluoride/stannous fluoride, clinical trial
Brief summary
The purpose of this study is to determine whether rinsing with an amine fluoride/stannous flouride mouthrinse in addition to daily tooth brushing is more effective than tooth brushing alone.
Detailed description
Gingivitis prevalence is 100% among the population. This is mostly due to an inadequate mechanical cleaning of the teeth. However, remaining dental biofilm can be approached by antibacterial mouthrinses. As a consequence of regular use of these mouthrinses, gingivitis can be reduced. Amine fluoride/stannous flouride mouthrinse (ASF)has proved its efficacy in several studies. In the previous years, a new formulation that does not contain ethanol anymore was introduced in the market. Therefore, it is the aim of the study to proof whether rinsing with ASF adjunctive to mechanical oral hygiene is more effective on gingivitis reduction than mechanical oral hygiene alone. In addition, effects on dental plaque, discoloration of teeth and bacterial colonization should be studied.
Interventions
DRUGamine fluoride/stannous fluoride
10 ml qd, oral, topical, 6 months duration
Sponsors
Gaba International AG
Technische Universität Dresden
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Healthy male and female adults aged ≥18 years. * Participants who have gingivitis/mild chronic periodontitis (approximal probing depth ≤ 3.5 mm at ≥ 80 % of the sites and at ≤ 20 % of the sites \> 3.5 mm and \< 5 mm). * Participants must have read, understood and signed the informed consent form. * Participants who have a GI ≥ 1.3 at baseline. * Participants who have at least 20 own teeth excluding the wisdom teeth (incl. 16 natural crowns). * Participants who have an acceptable compliance according to the investigators' assessment.
Exclusion criteria
* Participants who have systemic diseases that require regular systemic medication intake that may affect the gingival condition (e. g. phenytoin, nifedipine, cyclosporine, antibiotics, steroids, antiphlogistics). * Participants who require antibiotic treatments for dental appointments (endocarditis prophylaxis). * Participants who were treated with antibiotics 8 weeks before recruitment and during the course of the study. * Participants who were treated with any antibacterial mouthrinse 6 weeks before recruitment. * Participants who use other than the recommended mouthrinse or toothpaste during the study period. * Participants who have moderate and severe chronic or aggressive periodontitis. * Participants who have irregularities of the gingival tissues, e. g. hyperplastic gingiva, mucosal diseases. * Participants who have rampant caries. * Participants under guardianship or without freedom by administrative or legal award. * Known hypersensitivity or allergy to the study product and standard toothpaste ingredients used in the present study. * Known pregnancy or breast feeding during the course of the study. * Participation in another clinical trial or receipt of an investigational compound/treatment at the same time and 4 weeks prior to inclusion.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Reduction in gingivitis | 6 months | To proof whether rinsing with ASF adjunctive to mechanical oral hygiene is more effective on gingivitis reduction than mechanical oral hygiene alone. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Reduction in plaque | 6 months | To proof whether rinsing with ASF adjunctive to mechanical oral hygiene is more effective on plaque reduction than mechanical oral hygiene alone. |
| Discoloration of teeth | 6 months | To proof the effect of rinsing with ASF on discoloration of teeth |
| Bacterial colonization | 6 months | To proof whether rinsing with ASF adjunctive to mechanical oral hygiene influences bacterial colonization |
| Adverse events | 6 months | Recording all adverse events over the entire rinsing period |
Countries
Germany
Outcome results
None listed