CompletedNot Applicable

A Clinical Study to Evaluate the Efficacy of a Stannous Fluoride Dentifrice in the Relief of Dentinal Hypersensitivity in a Chinese Population

China271 participantsStarted 2021-07-27

Plain-language summary

The purpose of this study is to support long-term dentinal hypersensitivity (DH) relief claims of 0.454 percent (%) stannous fluoride (SnF2) containing toothpastes in China.

Who can participate

Age range18 Years – 70 Years

SexALL

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Inclusion criteria

✓. Self-reported history of dentinal hypersensitivity lasting more than six months but not more than 10 years.
✓. Good general oral health, with a minimum of 20 natural teeth.
✓. Minimum of 2 accessible non-adjacent teeth (incisors, canines, pre-molars), preferably in different quadrants, that meet all of the following criteria:

What they're measuring

Change From Baseline in Schiff Sensitivity Score at Week 8 (Test Dentifrice Versus [vs.] Negative Control)

Timeframe: Baseline and Week 8

Trial details

NCT IDNCT04950465

SponsorHALEON

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2022-01-25

Results submitted2022-12-19

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