Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02543060 · ClinicalTrials.gov registry record · NA

A Pilot Study to Evaluate a Method for Plaque When Comparing Stannous Fluoride Toothpaste to a Regular Dentifrice

A NA study of Gingivitis and Plaque, sponsored by Procter and Gamble.

Completed
Registry status
NA
Development phase
60
Enrollment target
1
Study location

NCT02543060: Completed NA study of Gingivitis and Plaque, sponsored by Procter and Gamble.

NCT02543060 is a NA study of Gingivitis and Plaque that has completed, run by Procter and Gamble. The registered enrollment target is 60 participants, below the 234-participant average among 25 other Gingivitis trials with a reported enrollment target (74% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02543060, a NA study of Gingivitis and Plaque, has completed, sponsored by Procter and Gamble.

COMPLETED
Registry status
NA
Development phase
60 participants
Enrollment target
1
Study location

Study Summary

This study will evaluate the sensitivity of an assay and its ability to split a marketed stannous fluoride toothpaste versus a negative control.

Conditions Studied

Interventions

  • DRUG stannous fluoride toothpaste
  • DRUG cavity protection toothpaste

Study Locations (1)

Indiana

  • Salus Research - Fort Wayne

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2015-06
Est. Completion 2015-08
Phase NA
Procter and Gamble

70 total trials

What the finished NCT02543060 record still lists

NCT02543060 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 234-participant average among 25 other Gingivitis trials with a reported enrollment target (74% lower).

The record links to 2 conditions, with Gingivitis appearing as the primary indexed condition, and to 2 interventions - of which stannous fluoride toothpaste is the first listed.

NCT02543060 reports a single indexed study location in Indiana.

Frequently Asked Questions

What is clinical trial NCT02543060 about?

NCT02543060 is a clinical study titled "A Pilot Study to Evaluate a Method for Plaque When Comparing Stannous Fluoride Toothpaste to a Regular Dentifrice". This study will evaluate the sensitivity of an assay and its ability to split a marketed stannous fluoride toothpaste versus a negative control.

What is the current status of trial NCT02543060?

This trial is currently completed. It is a NA study. The enrollment target is 60 participants. The study started on 2015-06. Estimated completion is 2015-08.

What conditions does trial NCT02543060 study?

This clinical trial studies the following conditions: Gingivitis, Plaque.

What interventions are being tested in trial NCT02543060?

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

Who is sponsoring clinical trial NCT02543060?

This trial is sponsored by Procter and Gamble, which has 70 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02543060 being conducted?

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

Similar trials for Gingivitis

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT02543060's enrollment target sits among peer trials

60 22nd of 25 higher than 4 of 25 other Gingivitis trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Gingivitis 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00576069 · 60 participants

    Mechanism(s)of Airflow Limitation in Moderate-severe Persistent Asthma

  • NCT01297400 · 60 participants · Phase 2

    Phase 2 Pilot Study of the Safety and Efficacy of Topical MW-III in Thermal Burns

  • NCT01734122 · 60 participants

    Stereotactic Radiosurgery for Essential Tremor and Parkinsonian Tremor

  • NCT01804634 · 60 participants · Phase 2

    Reduced Intensity Haploidentical BMT for High Risk Solid Tumors

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02543060, the US trial registry maintained by the National Library of Medicine. NCT02543060 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.