Evaluation of the Fluoride Dose Response Using In Situ Caries Model

PHASE4CompletedINTERVENTIONAL
Enrollment

15

Participants

Timeline

Start Date

March 1, 2021

Primary Completion Date

July 21, 2021

Study Completion Date

July 21, 2021

Conditions
Caries
Interventions
DRUG

0 ppm F

Each subject will be randomly assigned to this treatment during one of the four periods for this crossover study.

DRUG

250 ppm F as MFP

Each subject will be randomly assigned to this treatment during one of the four periods for this crossover study.

DRUG

1100 ppm as MFP

Each subject will be randomly assigned to this treatment during one of the four periods for this crossover study.

DRUG

2800 ppm F as MFP

Each subject will be randomly assigned to this treatment during one of the four periods for this crossover study.

DRUG

1100 ppm SnF2

Each subject will be assigned to this treatment during the fifth period for this crossover study.

Trial Locations (1)

46202

Oral Health Research Institute, Indianapolis

All Listed Sponsors
lead

Procter and Gamble

INDUSTRY

NCT04763044 - Evaluation of the Fluoride Dose Response Using In Situ Caries Model | Biotech Hunter | Biotech Hunter