Gingivitis Clinical Trial
Official title:
Study of the Anti-Inflammatory Effects of Colgate Total® During an Experimental Gingivitis Model
This study evaluates the anti-inflammatory effects of Colgate Total® during an experimental gingivitis model developed by Löe et al. Half of the participants will use Colgate Total® (which contains triclosan), while the other half will use a toothpaste which does not contain triclosan as the control.
This will be a double-blind. Subjects will be randomly assigned to the test or control
dentifrice arm. Enrolled subjects will also be randomly assigned to either right or left
side mandibular stent.
During the induction phase (i.e., day 0 to day 21), participants are instructed to refrain
from all hygiene procedures in the stent area. During this time period, participants evenly
distributed 2mL of their assigned dentifrice into their stent, allowing it to come into
contact with the areas of experimental gingivitis for two minutes twice daily while
traditional tooth brushing was performed in the non-stent areas. Clinical measures, saliva,
gingival crevicular fluid and plaque samples will be collected at days 0, 14, 21, and 35
study visits. A randomization chart will be used to identify which two sites (teeth and
tooth surface) will be used at the specific study visit for collection of gingival
crevicular fluid(GCF) and plaque.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor)
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