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NCT06660069 · ClinicalTrials.gov registry record · NA
A Study to Evaluate the Efficacy of a Stannous Fluoride Toothpaste With a Cetylpyridinium Chloride Mouthwash in Improving Gingival Health and Reducing Plaque Accumulation
A NA study of Gingivitis and Dental Plaque, sponsored by HALEON.
- Completed
- Registry status
- NA
- Development phase
- 199
- Enrollment target
- 1
- Study location
NCT06660069 is a NA study of Gingivitis and Dental Plaque that has completed, run by HALEON. The registered enrollment target is 199 participants, below the 229-participant average among 25 other Gingivitis trials with a reported enrollment target (13% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06660069, a NA study of Gingivitis and Dental Plaque, has completed, sponsored by HALEON.
- COMPLETED
- Registry status
- NA
- Development phase
- 199 participants
- Enrollment target
- 1
- Study location
Study Summary
The aim of this study is to assess the ability of a marketed Cetylpyridinium Chloride (CPC) mouthwash alongside a marketed Stannous Fluoride (SnF2) toothpaste in improving gingival health and reducing plaque accumulation, compared to the use of a regular fluoride toothpaste alone in participants with clinically measurable plaque-induced gingivitis.
Conditions Studied
Interventions
- DRUG Stannous Fluoride Toothpaste (Parodontax Complete Protection Toothpaste)
- DRUG CPC Mouthwash (Parodontax Active Gum Health Mouthwash)
- DRUG Regular Fluoride Toothpaste (Crest Cavity Protection)
Study Locations (1)
Indiana
- Salus Research - Fort Wayne
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 199 participants |
| Start Date | 2024-11-18 |
| Est. Completion | 2025-03-11 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06660069
The ClinicalTrials.gov registry entry for NCT06660069 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 199 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 229-participant average among 25 other Gingivitis trials with a reported enrollment target (13% lower). The listed sponsor is HALEON, which has 34 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Gingivitis appearing as the primary indexed condition, and to 3 interventions - of which Stannous Fluoride Toothpaste (Parodontax Complete Protection Toothpaste) is the first listed.
NCT06660069 reports 1 study location spanning 1 distinct geographic area - top geographies include Indiana.
Frequently Asked Questions
What is clinical trial NCT06660069 about?
NCT06660069 is a clinical study titled "A Study to Evaluate the Efficacy of a Stannous Fluoride Toothpaste With a Cetylpyridinium Chloride Mouthwash in Improving Gingival Health and Reducing Plaque Accumulation". The aim of this study is to assess the ability of a marketed Cetylpyridinium Chloride (CPC) mouthwash alongside a marketed Stannous Fluoride (SnF2) toothpaste in improving gingival health and reducing plaque accumulation, compared to the use of a regular fluoride toothpaste alone in participants wit...
What is the current status of trial NCT06660069?
This trial is currently completed. It is a NA study. The enrollment target is 199 participants. The study started on 2024-11-18. Estimated completion is 2025-03-11.
What conditions does trial NCT06660069 study?
This clinical trial studies the following conditions: Gingivitis, Dental Plaque.
What interventions are being tested in trial NCT06660069?
The interventions under investigation include: Stannous Fluoride Toothpaste (Parodontax Complete Protection Toothpaste) (DRUG), CPC Mouthwash (Parodontax Active Gum Health Mouthwash) (DRUG), Regular Fluoride Toothpaste (Crest Cavity Protection) (DRUG).
Who is sponsoring clinical trial NCT06660069?
This trial is sponsored by HALEON, which has 34 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06660069 being conducted?
This trial has 1 study location across Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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