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A Study to Evaluate the Dentinal Hypersensitivity Efficacy of Two Experimental Mouthwash Formulations

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NCT07741032

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

Phase
Not applicable
Status
Completed
Study type
Interventional
Design
Randomized · Single · Treatment
Enrollment
118actual
Sites
1
Country
Germany

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
Start2012-03-26actualWhen the study began enrolling
Primary completion2012-07-09actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2012-07-09actualThe whole study's end, after follow-up
First posted2026-08-03actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-03actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Dentine Hypersensitivity

Interventions

  • Other: 3% KNO3 Mouthwash
  • Other: 2% HPC Mouthwash
  • Other: 0% KNO3 Mouthwash

Primary outcomes

what the primary-completion date above is the date OF
Change From Baseline in Schiff Sensitivity Score at Weeks 4, 6 and 8
measured Baseline, Weeks 4, 6 and 8
Change From Baseline in Tactile Threshold at Weeks 4, 6 and 8
measured Baseline, Weeks 4, 6 and 8

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