Trials / Completed
CompletedNCT02192060
Efficacy of a Triclosan Formulation to Control the Initial Subgingival Biofilm Formation
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 28 (actual)
- Sponsor
- Federal University of Rio Grande do Sul · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The aim of the study is to compare the effect of a suspension containing Triclosan in dynamic of the subgingival biofilm formation versus a Placebo suspension. The initial subgingival biofilm formation will be evaluated by means of Plaque Free Zone (PFZ).
Detailed description
This is a double blind, cross over, randomized clinical trial. 28 volunteers will stop mechanical supragingiva biofilm removal measures for 96h following a complete scaling and polishing of the tooth surfaces. During this period they will be asked to rinse for one minute with a slurry of either a triclosan containing dentifice or a control without triclosan. Every 24h the presence of deposits will be registered with special atention to the presence of a plaque free zone between the apical border of the deposits and the gingival margin. Absence of deposits is scored 0, presence of deposits and plaque free zone =1 and presence of deposits and absence of plaque free zone =2 (MALISKA, A. N. et al. Measuring early plaque formation clinically. Oral health preventive dentistry, v. 4, p. 273-278, 2006). The prevalence of scores and the rate of changes from scores 0 and 1 into 2 will be evaluated for significance. Sample size was calculated taking the results from the study o MALISKA, AN (2006) as reference.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Test - Using of a suspension containing Triclosan | The participants should have used only the suspension containing Triclosan during 5 days and have stopped with their biofilm control homemade procedures. |
| OTHER | Control - Using of a suspension without Triclosan | The participants should have used only the Placebo suspension during 5 days and have stopped with their biofilm control homemade procedures. |
Timeline
- Start date
- 2013-05-01
- Primary completion
- 2013-06-01
- Completion
- 2013-06-01
- First posted
- 2014-07-16
- Last updated
- 2014-07-16
Locations
1 site across 1 country: Brazil
Source: ClinicalTrials.gov record NCT02192060. Inclusion in this directory is not an endorsement.