Evaluation of a Toothpaste Containing a Gum Health Active in Participants With Gingival Problem
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUnilever R&D
About this trial
The primary objective of this clinical study is to evaluate the impact on gingival health when participants switch to a fluoride toothpaste without gum-health actives for 4 weeks after using a proven gum-health toothpaste for 13 weeks.
Eligibility criteria
Qualifiers
Participants need to be competent i.e., able to understand what is to take place and able to provide a free decision on agreeing to the activity/taking part in the study on this.
Participants must be able to read and understand study instructions and any other relevant study documents.
Have at least 20 natural teeth without subgingival calculus, including 5 assessable teeth (excluding 3rd molars) in each quadrant.
Have a mean whole mouth BOP ≥ 10% at screening.
Disqualifiers
Be pregnant or breastfeeding.
Participants who participated in gum health study within 3 months prior to screening.
Current participation in any other cosmetic studies, any dental clinical studies or clinical trials.
Participants who have used any gum health products in the 4 weeks prior to screening.
Trial design
Treatments tested in this trial
- Test Toothpaste
- Control Toothpaste
Treatment groups
150 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov