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Completed

NCT Number: NCT07428603

Extrinsic Tooth Whitening Evaluation of a Whitening Toothpaste

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.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Salus Research, Inc.

Fort Wayne, Indiana, 46825, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Whitening Test Dentifrice (Code 826)

Other

Whitening toothpaste used twice daily for two minutes per brushing for six weeks.

Control dentifrice (Code 378)

Other

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

Primary outcomes

  1. 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

  1. Change in Stain Intensity and Stain Area Scores

    Time frame: Baseline to Days 7, 14, 28, and 42

    Mean changes in stain intensity and stain area scores at each post-baseline time point.

Other outcomes

  1. Subject-Reported Whitening and Sensory Assessments

    Time frame: Baseline and Days 7, 14, 28, and 42

    Subject-reported perceptions of whitening, mouthfeel, and sensory responses collected via questionnaires.

Sponsors and collaborators

Lead sponsor

Church & Dwight Company, Inc.

Industry

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Feb 24, 2026
Registry last updated
Feb 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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