Clinical Trials Directory

Trials / Completed

CompletedNCT02752958

Impact of Long Term Management of Dentine Hypersensitivity (DH) With a Daily Use Anti-sensitivity Toothpaste on the Quality of Life Related to Oral Health

Study to Investigate the Impact on Oral Health Related Quality of Life of Managing Dentine Hypersensitivity With a Daily Use Anti-Sensitivity Toothpaste

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
75 (actual)
Sponsor
GlaxoSmithKline · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

This multicentre, non-comparative design study will monitor the impact of long term management of DH with daily use of a sensitivity toothpaste on the quality of life of a population of sensitivity sufferers. Changes in oral health related quality of life will be monitored using the Dentine Hypersensitivity Experience Questionnaire (DHEQ). The study will be conducted in participants in good general health, with pre-existing self-reported and clinically diagnosed tooth sensitivity at screening.

Detailed description

This will be multicenter, non-comparative design to monitor the impact of long term management of DH with daily use of a sensitivity toothpaste on the quality of life of a population of sensitivity sufferers, using the DHEQ. Changes in DH will be monitored clinically over the 24 week treatment period.

Conditions

Interventions

TypeNameDescription
DRUGstannous fluoride0.454% w/w (weight per weight) stannous fluoride

Timeline

Start date
2016-05-23
Primary completion
2017-02-01
Completion
2017-02-03
First posted
2016-04-27
Last updated
2018-08-27
Results posted
2018-08-27

Locations

2 sites across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT02752958. Inclusion in this directory is not an endorsement.