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Clinical Trials/NCT07428603
NCT07428603
Completed
Not Applicable

Six-Week Clinical Evaluation of a Toothpaste in Tooth Whitening Via Extrinsic Stain Removal

Church & Dwight Company, Inc.1 site in 1 country118 target enrollmentStarted: August 8, 2024Last updated:

Overview

Phase
Not Applicable
Status
Completed
Sponsor
Church & Dwight Company, Inc.
Enrollment
118
Locations
1
Primary Endpoint
Change in Extrinsic Tooth Stain (Total Stain Score)

Overview

Brief Summary

This randomized, examiner-blind, parallel-group clinical study evaluated the effectiveness of a whitening toothpaste compared with a control toothpaste in removing extrinsic tooth stain over six weeks of twice-daily unsupervised use. Adult subjects were assessed at baseline and after 7, 14, 28, and 42 days of product use using the Macpherson Modification of the Lobene Stain Index. Oral soft and hard tissues and subject-reported sensory responses were also evaluated throughout the study.

Detailed Description

This single-site, randomized, examiner-blind, two-cell parallel clinical trial enrolled adult subjects with qualifying extrinsic tooth stain. Following baseline assessments, subjects were randomized to either a test whitening dentifrice or a marketed control dentifrice. Subjects brushed twice daily for two minutes with their assigned toothpaste and toothbrush for 42 days. Extrinsic stain on the labial surfaces of the 12 anterior teeth was evaluated at baseline and at Days 7, 14, 28, and 42 using the Macpherson Modification of the Lobene Stain Index, assessing stain intensity, stain area, and total stain scores. Safety was monitored via oral soft and hard tissue examinations and subject-reported sensory assessments. Treatment comparisons were performed using ANCOVA with baseline scores as covariates.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Adults 18-65 years in good general health
  • Mean MLSI score ≥1.5 on labial surfaces of at least 8 of 12 anterior teeth
  • Adequate oral hygiene and willingness to comply with study requirements
  • Dental prophylaxis within past 18 months but not within past 3 months
  • Willing to refrain from other whitening or oral care products during the study

Exclusion Criteria

  • Significant medical conditions or oral pathology affecting assessments
  • History of adverse reactions to oral hygiene products
  • Orthodontic appliances or restorations interfering with stain assessment
  • Moderate or advanced periodontitis
  • Recent bleaching or whitening treatments
  • Pregnant or nursing

Arms & Interventions

Test Toothpaste

Experimental

Investigational whitening toothpaste evaluated for removal of extrinsic tooth stain over 42 days of use.

Intervention: Whitening Test Dentifrice (Code 826) (Other)

Sodium Fluoride Control Dentifrice

Other

Non-whitening toothpaste used twice daily for two minutes per brushing for six weeks.

Intervention: Control dentifrice (Code 378) (Other)

Outcomes

Primary Outcomes

Change in Extrinsic Tooth Stain (Total Stain Score)

Time Frame: Baseline to Day 42

Mean change in total extrinsic stain score measured on the labial surfaces of the 12 anterior teeth using the Macpherson Modification of the Lobene Stain Index, combining stain intensity and stain area scores.

Secondary Outcomes

  • Change in Stain Intensity and Stain Area Scores(Baseline to Days 7, 14, 28, and 42)

Investigators

Sponsor
Church & Dwight Company, Inc.
Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (1)

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