drugset / Trial / NCT07263698
Investigation of Clinical Efficacy of a New Mouthwash on Reducing Dental Plaque and Helping Prevent Gum Problems as Compared to a Control Mouthwash
RandomizedParallel-groupQuadruple-blindTreatment
Summary
Qualified subjects will be enrolled and randomized to either one of the two study groups described above based on their initial modified gingivitis and plaque scores. Subjects will be instructed to use the products according to the instructions provided. Subjects will return to the dental office for evaluation after two weeks, six weeks and three months of product use. All subjects will be followed for adverse events throughout the study
Timeline
- Start
- 2025-12-01
- Primary completion
- 2026-02-27
- Completion
- 2026-02-27
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Cetylpyridinium | Small molecule | 0.09 % | — |
| Subject | Zinc Lactate | Unknown | 0.28 % | — |
| Comparator | sodium fluoride | Unknown | 100 ppm | — |
| Comparator | sodium fluoride | Unknown | 500 ppm | — |