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

NCT07149376 · ClinicalTrials.gov registry record · Phase 3

To Assess the Efficacy of a Toothpaste Containing 8% Arginine as Compared to Colgate Cavity Protection Toothpaste in the Reduction of Dentinal Hypersensitivity.

A Phase 3 study, sponsored by Colgate Palmolive.

Completed
Registry status
Phase 3
Development phase
84
Enrollment target

NCT07149376: Completed Phase 3 study, sponsored by Colgate Palmolive.

NCT07149376 is a Phase 3 study that has completed, run by Colgate Palmolive. The registered enrollment target is 84 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (89% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT07149376, a Phase 3 study, has completed, sponsored by Colgate Palmolive.

COMPLETED
Registry status
Phase 3
Development phase
84 participants
Enrollment target

Study Summary

The objective of this clinical investigation is to assess the efficacy of a toothpaste containing 8% arginine (Colgate-Palmolive Company, New York, NY, USA) as compared to a commercially available non-desensitizing toothpaste (Colgate Cavity Protection Toothpaste, Colgate-Palmolive Company, New York, NY, USA) in the reduction of dentinal hypersensitivity over an eight (8) week period.

Primary Outcome

Hypersensitivity defined by a response score in the range of 10-50 grams of force.

Interventions

  • DEVICE TOMs of Maine Sensitive SLS Free Xtra Fresh
  • DRUG Colgate Cavity protection toothpaste

Trial Details

FieldValue
Enrollment Target 84 participants
Start Date 2025-08-18
Est. Completion 2025-10-14
Phase Phase 3
Colgate Palmolive

51 total trials

What the finished NCT07149376 record still lists

NCT07149376 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 84 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (89% lower).

The record links to 0 conditions, and to 2 interventions - of which TOMs of Maine Sensitive SLS Free Xtra Fresh is the first listed.

NCT07149376 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07149376 about?

NCT07149376 is a clinical study titled "To Assess the Efficacy of a Toothpaste Containing 8% Arginine as Compared to Colgate Cavity Protection Toothpaste in the Reduction of Dentinal Hypersensitivity.". The objective of this clinical investigation is to assess the efficacy of a toothpaste containing 8% arginine (Colgate-Palmolive Company, New York, NY, USA) as compared to a commercially available non-desensitizing toothpaste (Colgate Cavity Protection Toothpaste, Colgate-Palmolive Company, New York...

What is the current status of trial NCT07149376?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 84 participants. The study started on 2025-08-18. Estimated completion is 2025-10-14.

What interventions are being tested in trial NCT07149376?

The interventions under investigation include: TOMs of Maine Sensitive SLS Free Xtra Fresh (DEVICE), Colgate Cavity protection toothpaste (DRUG).

Who is sponsoring clinical trial NCT07149376?

This trial is sponsored by Colgate Palmolive, which has 51 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07149376's enrollment target sits among peer trials

84 1749th of 2000 higher than 250 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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

  • NCT02391519 · 84 participants

    Effects of High Altitude on AMPK Activation

  • NCT03838536 · 84 participants · NA

    Synergistic Activity of Human Milk Nutrients and Infant Cognition

  • NCT03884075 · 84 participants · Phase 2

    Non-Alcoholic Fatty Liver Disease, the HEpatic Response to Oral Glucose, and the Effect of Semaglutide (NAFLD HEROES)

  • NCT03894917 · 84 participants

    Characterizing Disease Biology, Treatment and Toxicity in Older Adults With Hepatocellular Carcinoma

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT07149376, the US trial registry maintained by the National Library of Medicine. NCT07149376 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.