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A Clinical Study to Assess the Efficacy of a Calcium Sodium Phosphosilicate Toothpaste for the Relief of Dentine Hypersensitivity

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NCT07802886 · readout ≤ 208 d

Sponsored by HALEON (industry) · HLN — their whole pipeline →.

Phase
Not applicable
Status
Not yet recruiting
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
192estimated
Sites
1
Country
United Kingdom

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-09-03

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
StartSep 2026estimatedWhen the study began enrolling
Primary completionMar 2027estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionMar 2027estimatedThe whole study's end, after follow-up
First posted2026-09-03actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-09-03actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Dentin Sensitivity

Interventions

  • Device: Test Toothpaste
  • Other: Regular Fluoride Toothpaste

Primary outcome

what the primary-completion date above is the date OF
Change from Baseline in Schiff Sensitivity Score at Week 8
measured Baseline and Week 8

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