Trials / Recruiting
RecruitingNCT07300540
Real-World Study of a Calcium Sodium Phosphosilicate Anti-Sensitivity Toothpaste for Dentin Hypersensitivity Relief
A Real-World Evidence Study Evaluating Oral Health Related Quality of Life With Use of a Calcium Sodium Phosphosilicate Anti-Sensitivity Dentifrice for Dentin Hypersensitivity Management
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 500 (estimated)
- Sponsor
- HALEON · Industry
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Accepted
Summary
The aim of this study is to evaluate the impact of a commercially available desensitizing dentifrice containing 5 percent (%) Calcium sodium phosphosilicate (CSPS) on oral health related quality of life (OHrQoL) in a DH (Dentin Hypersensitivity) population in a real-world setting.
Detailed description
This will be a decentralized, prospective, 24-week, monadic design, open label, study in a DH population. The study will evaluate changes in OHrQoL in participants with self-reported DH symptoms. OHrQoL will be measured using a validated questionnaire, the Dentin Hypersensitivity Experience Questionnaire (DHEQ-48), completed by study participant. Sufficient numbers will be screened to enroll approximately 500 participants to ensure approximately 400 evaluable participants complete the entire study.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Calcium sodium phosphosilicate (CSPS) Toothpaste | A toothpaste containing 5% weight/weight (w/w) calcium sodium phosphosilicate. |
Timeline
- Start date
- 2026-03-04
- Primary completion
- 2026-11-01
- Completion
- 2026-11-01
- First posted
- 2025-12-23
- Last updated
- 2026-03-11
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT07300540. Inclusion in this directory is not an endorsement.