NCT07415733 Evaluation of a Toothpaste Containing a Gum Health Active in Participants With Gingival Problem
| NCT ID | NCT07415733 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Unilever R&D |
| Condition | Gingival Inflammation |
| Study Type | INTERVENTIONAL |
| Enrollment | 150 participants |
| Start Date | 2026-02-27 |
| Primary Completion | 2026-07 |
Trial Parameters
Eligibility Fast-Check
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Brief Summary
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
Inclusion Criteria: * 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. * Willing to follow the lifestyle and dietary restrictions as detailed in the Information Sheet for study. Exclusion Criteria: * 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. * Obvious signs of untreated caries or significant periodontal disea