Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Dental Caries
  • Dental Erosion
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Crossover AssignmentIntervention Model Description: Total of 9 arms initially, and later the study will concentrate on 5 amrsMasking: Double (Participant, Care Provider)Masking Description: Mouth rinses will be placed in coded bottles, and the investigator and patients will not know to which group they belong.Primary Purpose: Prevention

Participation Requirements

Age
Between 18 years and 45 years
Gender
Both males and females

Description

This study will be made in three in situ parts. Participants will wear an oral appliance containing sterilized enamel and dentine slabs. During this experimental phase, they will use the designated mouth rinse. After this period, the investigators will remove the enamel and dentine slabs, and will a...

This study will be made in three in situ parts. Participants will wear an oral appliance containing sterilized enamel and dentine slabs. During this experimental phase, they will use the designated mouth rinse. After this period, the investigators will remove the enamel and dentine slabs, and will also collect salivary pellicle and any bacterial biofilm forming on the participant's teeth. Participants will also donate saliva for proteomic analysis (protein profile) to verify if there are any differences in proteins in saliva to proteins in the pellicle. Throughout the whole study, all participants will use standardized oral hygiene products. The experimental mouth rinses contain plant extracts that could interact with salivary proteins and influence the salivary pellicle and oral biofilm, thus bringing positive results against tooth (enamel and dentine) demineralisation.

Tracking Information

NCT #
NCT04033263
Collaborators
Not Provided
Investigators
Principal Investigator: Thiago S Carvalho, PD Dr University of Bern