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Exploratory Clinical Study to Investigate the Ability of an Experimental Combination Dentifrice to Protect Sensitive Teeth

NCT05243745 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2024-09-20

Study results available
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Summary

This proof of principle (PoP) study will evaluate the ability of an experimental combination toothpaste formulation to protect sensitive teeth from dentine hypersensitivity.

Conditions

  • Dentin Sensitivity

Interventions

OTHER

3% PVM/MA + 5% KNO3 Combination

Toothpaste containing 3% PVM/MA + 5% KNO3 as combination will be used as test product.

OTHER

3% PVM/MA only

Toothpaste containing 3% PVM/MA only will be used as comparator 1 product.

OTHER

5% KNO3 Only

Toothpastes containing 5% KNO3 only will be used as comparator 2 product.

OTHER

Regular Fluoride

Toothpaste containing regular fluoride will be used as negative control.

Sponsors & Collaborators

  • HALEON

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-02-28
Primary Completion
2022-10-03
Completion
2022-10-03

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05243745 on ClinicalTrials.gov