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Clinical Study to Evaluate Remineralization Using an in Situ Model.

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NCT07625670 · readout ≤ 73 d

Sponsored by Colgate Palmolive (industry) · CL — their whole pipeline →. With Federal University of Paraíba.

Phase
Phase 3
Status
Not yet recruiting
Study type
Interventional
Design
Randomized · Quadruple · Other
Enrollment
30estimated
Sites
1
Country
Brazil

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
StartJun 2026estimatedWhen the study began enrolling
Primary completionOct 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionOct 2026estimatedThe whole study's end, after follow-up
First posted2026-06-04actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-06-04actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Remineralization
  • Enamel Lesions
  • Enamel Subsurface Lesion

Interventions

  • Drug: Fluoride toothpaste containing 750 ppm MFP in a Dical base
  • Drug: Fluoride toothpaste containing 1450 ppm MFP in a Dical base
  • Drug: Fluoride-free toothpaste in a Dical base
  • Device: Toothbrush

Primary outcome

what the primary-completion date above is the date OF
Change in integrated mineral loss (Δz)
measured 9 weeks

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