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To Assess the Efficacy of a Toothpaste Containing 8% Arginine as Compared to Colgate Cavity Protection Toothpaste in the Reduction of Dentinal Hypersensitivity.

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NCT07149376

Sponsored by Colgate Palmolive (industry) · CL — their whole pipeline →.

Phase
Phase 3
Status
Completed
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
84actual
Sites
1
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
Start2025-08-18actualWhen the study began enrolling
Primary completion2025-10-14actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-10-14actualThe whole study's end, after follow-up
First posted2025-09-02actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-11-05actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Sensitivity, Tooth

Interventions

  • Device: TOMs of Maine Sensitive SLS Free Xtra Fresh
  • Drug: Colgate Cavity protection toothpaste

Primary outcomes

what the primary-completion date above is the date OF
Tactile stimulation by the Yeaple Probe
measured baseline, 3 day, 4 weeks, 8 weeks
Air blast stimulation
measured baseline, 3 day, 4 weeks, 8 weeks

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