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RECRUITING Phase 3

Efficacy of a Stannous Fluoride Toothpaste, Cetylpyridinium Chloride Mouthwash, and Battery Toothbrush Regimen in Reducing Established Dental Plaque and Gingivitis.

NCT07398846 · View on ClinicalTrials.gov ↗

Study Summary

To evaluate the efficacy of a stannous fluoride toothpaste, Cetylpyridinium Chloride Mouthwash, and Battery Toothbrush Regimen in Reducing Established Dental Plaque and Gingivitis.

Conditions Studied

Interventions

  • DRUG 0.454%Stannous fluoride toothpaste
  • DRUG 0.075% Cetylpyridinium Chloride (CPC) and 0.28% zinc lactatmouthwashe
  • DRUG 0.76% Sodium Monofluorophosphate (Na MFP) toothpaste
  • DRUG 0.022% Sodium Fluoride mouthwash

Study Locations (1)

Florida

  • Consumer Research Consulting, LLC — Melbourne

Trial Details

FieldValue
Enrollment Target 135 participants
Start Date 2026-01-26
Est. Completion 2026-04-20
Phase Phase 3

Sponsor

Colgate Palmolive

9 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07398846

The ClinicalTrials.gov registry entry for NCT07398846 describes a study currently listed as recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 135 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Colgate Palmolive, which has 9 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Plaque appearing as the primary indexed condition, and to 4 interventions — of which 0.454%Stannous fluoride toothpaste is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07398846 reports 1 study location spanning 1 distinct geographic area — top geographies include Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07398846 about?

NCT07398846 is a clinical study titled "Efficacy of a Stannous Fluoride Toothpaste, Cetylpyridinium Chloride Mouthwash, and Battery Toothbrush Regimen in Reducing Established Dental Plaque and Gingivitis.". To evaluate the efficacy of a stannous fluoride toothpaste, Cetylpyridinium Chloride Mouthwash, and Battery Toothbrush Regimen in Reducing Established Dental Plaque and Gingivitis.

What is the current status of trial NCT07398846?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 135 participants. The study started on 2026-01-26. Estimated completion is 2026-04-20.

What conditions does trial NCT07398846 study?

This clinical trial studies the following conditions: Plaque. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07398846?

The interventions under investigation include: 0.454%Stannous fluoride toothpaste (DRUG), 0.075% Cetylpyridinium Chloride (CPC) and 0.28% zinc lactatmouthwashe (DRUG), 0.76% Sodium Monofluorophosphate (Na MFP) toothpaste (DRUG), 0.022% Sodium Fluoride mouthwash (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07398846?

This trial is sponsored by Colgate Palmolive, which has 9 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07398846 being conducted?

This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial