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NCT06359028 · ClinicalTrials.gov registry record · NA

Clinical Study to Evaluate the Anti-sensitivity Efficacy of a Stannous Fluoride Toothpaste in a Population of Dentin Hypersensitivity Sufferers

A NA study, sponsored by HALEON.

Completed
Registry status
NA
Development phase
111
Enrollment target

NCT06359028: Completed NA study, sponsored by HALEON.

NCT06359028 is a NA study that has completed, run by HALEON. The registered enrollment target is 111 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06359028, a NA study, has completed, sponsored by HALEON.

COMPLETED
Registry status
NA
Development phase
111 participants
Enrollment target

Study Summary

The aim of this study is to confirm the clinical Dentin Hypersensitivity (DH) efficacy of a 0.454 percent (%) Stannous Fluoride (SnF2) toothpaste.

Primary Outcome

Schiff sensitivity score was assessed by participant's response to an evaporative (air) stimulus after the stimulation of the 2 test teeth selected at Baseline by the examiner. Participant's response to the stimulus was evaluated by the examiner using the Schiff sensitivity scale immediately following administration of the evaporative air stimulus. Score ranged from 0-3, where 0=Does not respond to air stimulation; 1=Responds to air stimulus but does not request discontinuation of stimulus; 2=Re

Interventions

  • DRUG Stannous fluoride toothpaste
  • DRUG Crest cavity protection toothpaste

Trial Details

FieldValue
Enrollment Target 111 participants
Start Date 2024-03-25
Est. Completion 2024-06-20
Phase NA
HALEON

34 total trials

What the finished NCT06359028 record still lists

NCT06359028 is an interventional study that assigns participants to a tested intervention. The registered 111 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 2 interventions - of which Stannous fluoride toothpaste is the first listed.

NCT06359028 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06359028 about?

NCT06359028 is a clinical study titled "Clinical Study to Evaluate the Anti-sensitivity Efficacy of a Stannous Fluoride Toothpaste in a Population of Dentin Hypersensitivity Sufferers". The aim of this study is to confirm the clinical Dentin Hypersensitivity (DH) efficacy of a 0.454 percent (%) Stannous Fluoride (SnF2) toothpaste.

What is the current status of trial NCT06359028?

This trial is currently completed. It is a NA study. The enrollment target is 111 participants. The study started on 2024-03-25. Estimated completion is 2024-06-20.

What interventions are being tested in trial NCT06359028?

The interventions under investigation include: Stannous fluoride toothpaste (DRUG), Crest cavity protection toothpaste (DRUG).

Who is sponsoring clinical trial NCT06359028?

This trial is sponsored by HALEON, which has 34 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06359028's enrollment target sits among peer trials

111 816th of 2000 higher than 1,185 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06359028, the US trial registry maintained by the National Library of Medicine. NCT06359028 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.