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Clinical Trial Summary

The purpose of this study is to evaluate changes in oral health-related quality of life (OHrQoL) in participants suffering from Dentinal Hypersensitivity (DH) symptoms following the use of anti-sensitivity toothpaste for 24 weeks.


Clinical Trial Description

This study will be a virtual, prospective, twenty-four weeks, open label study in participants with DH (self-reported symptoms). Participants self-perception of DH will be evaluated by completion of a validated OHrQoL questionnaire (Dentin Hypersensitivity Experience Questionnaire-48 [DHEQ-48]) at baseline, 4, 8, 12, 16, 20 and 24 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04964063
Study type Interventional
Source HALEON
Contact
Status Completed
Phase N/A
Start date August 31, 2021
Completion date May 13, 2022

See also
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