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Clinical Trial Summary

The study design is a randomised, split mouth, blind with respect to study analysts (microscopist, image grader) two treatment clinical study in 10 healthy participants with sound tooth enamel. The study will comprise of a screening visit, pre-baseline visit and 5 subsequent clinic visits. At the screening visit, participants will give consent to participate in the study. Medical history and concomitant medications will be recorded. Eligibility will be determined following an oral soft tissue (OST) examination and an evaluation of dentition exclusions. Two suitable anterior teeth will be identified for study assessments, these teeth must be at least one tooth apart in the mouth. Saliva samples will be collected from the participants at set points during the study to look at any changes in salivary pH.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02676219
Study type Interventional
Source Unilever R&D
Contact
Status Completed
Phase N/A
Start date July 1, 2015
Completion date September 18, 2015

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