drugset / Trial / NCT02194023
Clinical Effects of Two New Chlorhexidine Digluconate Formulations: 0.12% and 0.03%.
RandomizedParallel-groupQuadruple-blindSupportive care
Summary
In the current study we tested the hypothesis that new 0.05% Cetylpyridinium chloride (CPC) mouthrinse formulations containing 0.12% or 0.03% chlorhexidine digluconate (CHX): 1) yield similar or better clinical results regarding the inhibition of de novo plaque growth compared to those achieved with an already marketed 0.12% CHX mouthrinse (Perio-Aid Treatment without alcohol. Dentaid, Spain), 2) reduce the side effects caused by the marketed 0.12% CHX formula and 3) that these mouthrinses have no negative microbiological effects, and they control total bacterial loads.
Timeline
- Start
- 2011-09
- Primary completion
- 2013-07
- Completion
- 2013-07
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Cetylpyridinium | Small molecule | 0.05 % | Oral |
| Subject | Chlorhexidine gluconate | Other / unclassified | 0.03 % | Oral |
| Subject | Chlorhexidine gluconate | Other / unclassified | 0.12 % | Oral |