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Not yet recruitingNCT07124533Updated Jul 10, 2026

Effectiveness of Toothpaste Tablets on Plaque, Gingival Health and Caries Experiences

A Phase 3 interventional study of Toothpaste Tablet and Conventional Toothpaste in Gingival Inflammation and Dental Caries, sponsored by Loma Linda University. Not yet recruiting at 2 sites in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-10.

Sponsored by Loma Linda University · Phase 3, Interventional, and Prevention

Phase
Phase 3
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Objectives: To evaluate the effectiveness of toothpaste tablets when compared to conventional dentifrices in removing plaque.

Methods: 50 participants are randomized into two groups: Denttabs toothpaste tablets (T) and Colgate's Cavity Protection toothpaste (P). Both groups utilize their assigned dentifrice for 6 weeks. A pre and post-assessment measures the Gingival Index (GI) and Plaque Index (PI) and Decayed, Missing and Filled Teeth (DMFT). A questionnaire on the use of the product is distributed at the end of the study.

02

Conditions studied

  • Gingival Inflammation
  • Dental Caries

Keywords

  • Gingival Index
  • Plaque Index
  • Dentifrice
  • Toothpaste Tablets
  • Caries Experiences
  • Consumer Satisfaction
03

In context

Gingivitis

631 studies on the registry are indexed under Gingivitis; 107 are open to participants now.

This study's planned enrollment of 50 is below the median of 66 across 507 interventional studies indexed under Gingivitis.

Browse Gingivitis studies →

Lead sponsor

Loma Linda University is the lead sponsor of 306 studies on the registry; 46 are open to participants now.

Of its 29 completed or terminated interventional studies of FDA-regulated products, 23 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Subjects are 18 years or older;
  2. Subjects who will comply with study protocol;
  3. Subjects who can read and understand the consent form;
  4. Subjects available during the study period;
  5. Subjects have more than 20 teeth.

Exclusion criteria

Exclusion Criteria:

1. Subjects under the age of 18.

05

Study design

Phase
Phase 3
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Investigator)
Enrollment
50 participants (estimated)

Study arms

  • Experimental
    Toothpaste Tablet

    Subjects are instructed to use one toothpaste tablet at each brushing. Brushing is recommended twice daily for two minutes.

    Drug: Toothpaste Tablet

  • Active comparator
    Conventional Toothpaste

    Subjects are instructed to use the toothpaste at each brushing. Brushing is recommended twice daily for two minutes.

    Drug: Conventional Toothpaste

Interventions

06

What researchers measure

Primary outcomes

  1. Plaque Index Score at Baseline

    The quantity of plaque build-up is measured visually using the Quigley-Hein Plaque Index. The Plaque index can range from 0 to 5, with higher numbers indicating more plaque build-up.

    Time frame: Change between baseline at visit 1 and visit 2, six weeks post baseline

  2. Gingival Index Score at Baseline

    The severity of gingival inflammation is measured visually using the Loe-Silness Gingival Index. Gingival index can range from 0 to 3, with higher numbers indicating more gingival inflammation.

    Time frame: Change between baseline at visit 1 and visit 2, six weeks post baseline

Secondary outcomes

  1. DMFT Score at Baseline

    Caries experiences is measured visually using the DMFT index. DMFT score can range from 0 to 28, with higher numbers indicating higher caries experiences.

    Time frame: Change between baseline at visit 1 and visit 2, six weeks post baseline

  2. Subject Perception of Product Use

    The perception on the product usage is measured using a survey containing questions on feel, texture, flavor, ease of use, eco-friendliness, cost and overall satisfaction. Response is on a 4 point Likert scale ranging from strongly agree (1) to strongly disagree (4).

    Time frame: Visit 2 six weeks post study enrollment

07

Study locations

2 sites
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07124533
Responsible party
Sponsor
First posted
Aug 15, 2025
Start date
Dec 2026 (estimated)
Primary completion
Dec 2026 (estimated)
Completion
Dec 2026 (estimated)
Last update
Jul 10, 2026

Study contacts

So Ran Kwon, DDS, MS, PhD
Contact
sorankwon@llu.edu
909 558 5118 ext. 55118
So Ran Kwon, DDS, MS, PhD
principal investigator · Loma Linda University

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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Studies of the drug tested here: Toothpaste

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