Dentine Sensitivity Clinical Trial
Official title:
A Pilot Study to Substantiate the Use of the Jay Sensitivity Sensor Probe by Correlating the Results With the Those of Yeaple Probe, Schiff Air Blast, Visual Analogue Scale (VAS) and Oral Health Impact Profile Questionnaire (OHIP)
Subjects with at least two teeth with dentinal hypersensitivity and who meet the study
criteria will be enrolled onto this double blind, randomised, parallel, controlled clinical
trial. After enrolment, suitable subjects will use a fluoride toothpaste for 4 weeks (wash
out period). Baseline dentine hypersensitivity assessments will be conducted using tactile
stimuli, air blast, and VAS methods. Tactile methods of assessment will include use of the
Yeaple Probe and the Jay Sensitivity Sensor probe. Air blast assessments will be conducted
using the Schiff cold air sensitivity scale. The Oral Health Impact Profile (OHIP)
questionnaire will be completed at four defined time points during the study. The baseline
assessments will be conducted on the two teeth identified during the screening visit.
On completion of the baseline assessments, subjects will be randomly assigned to product.
Dentinal hypersensitivity assessments will be repeated after 18, 28 and 56 days of product
use.
n/a
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT02371616 -
Clinical Study to Evaluate the Efficacy of Two Dentifrices for Dentine Hypersensitivity
|
N/A |