Real-World Study of a Calcium Sodium Phosphosilicate Anti-Sensitivity Toothpaste for Dentin Hypersensitivity Relief
Running, not enrolling · Not applicable
Conditions studied: Dentin Sensitivity
In brief
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.
Key facts
- Study ID
- NCT07300540
- Run by
- HALEON
- People needed
- 500
- Starts
- 2026-03-04
- Expected to finish
- 2026-11-01
- Last updated by the study team
- 2026-07-21
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Participant who has provided consent indicating they have been informed of all pertinent aspects of the study.
- All genders who, at the time of screening, are aged 18 to 65.
- Participant who is able to independently complete all activities on their smart devices
- Participant who has tooth sensitivity (self-reported symptoms).
You may not qualify if…
- Participants whose tooth sensitivity could be caused by other factors or clinical pathology than DH, as self-reported on the screening questionnaire, which include:
- Participant who has been/is on multiple prescription medications to treat severe acid reflux on a regular basis or has had surgery for acid reflux.
- Participant with full or partial denture.
- Participant who has undergone treatment for periodontal or gum disease within 6 months of screening or is currently undergoing treatment for periodontal or gum disease.
- Participant who has been informed by a Dental Health Care Professional (DHCP) that they have active periodontitis.
- Participants who have been informed by a DHCP that they have active caries.
- Participant with any chronic and/or severe painful health condition which lead to regular use of pain relief medications (more than 3 days a week).
- Participant with known or suspected intolerance or hypersensitivity to the study materials (or closely related compounds) or any of their stated ingredients.
Where it is running
- Citruslabs (Virtual Site) — Las Vegas, Nevada, United States
Full record on ClinicalTrials.gov
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