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Clinical Study to Investigate the Antihypersensitivity Efficacy of a Novel Dentifrice

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NCT07215767 · readout ≤ 11 d

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

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
688actual
Sites
3
Country
United States

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 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-09-16actualWhen the study began enrolling
Primary completionAug 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionAug 2026estimatedThe whole study's end, after follow-up
First posted2025-10-10actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-06-16actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Dentin Hypersensitivity

Interventions

  • Drug: Stannous fluoride and Potassium nitrate Dentifrice
  • Drug: Stannous fluoride Dentifrice
  • Drug: Potassium nitrate Dentifrice
  • Drug: Vehicle Dentifrice

Primary outcomes

what the primary-completion date above is the date OF
Change from Baseline in Schiff sensitivity score at Week 8 (Test Dentifrice Versus [Vs] Reference Dentifrices 1, 2 and 3)
measured Baseline and Week 8
Change from Baseline in tactile threshold (grams [g]) at Week 8 (Test Dentifrice Vs Reference Dentifrices 1, 2 and 3)
measured Baseline and Week 8

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