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Clinical Trials/NCT06800443
NCT06800443CompletedNot Applicable

A Cosmetic Study to Measure the Change in Tooth Colour After Using Instant Whitening Prototypes Compared to a Negative Control

Unilever R&D1 site in 1 country68 target enrollmentStarted: December 3, 2018Last updated:
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
68
Locations
1
Primary Endpoint
Tooth whiteness index (WIO) (average value from two upper central incisors

Study Overview

Brief Summary

This will be a double blind, randomised, four-group crossover study. This study will involve 5 visits to the study site, with a wash-out period of 1 week between visits. Visit 1 will be for screening, participants who meet inclusion and exclusion criteria (including having Vita shade score of 2M2, 3R1.5, 2R2.5, 3L1.5, 2L2.5, 4M1, 2M3, 3M2, 4R1.5, 4L1.5, 3L2.5, 3R2.5, 5M1, 4M2, 3M3 from VITA 3D-MASTER Shade Guide) will be accepted onto the study. At each test visit (visit 2 - 5), participants will have images taken of their front upper incisors using a a Video-based Digital Imaging System (VDIS) pre- and post-brushing with randomly allocated test or control toothpaste [1.5g for 90 seconds, followed by water rinse]. The digital images will be analysed using the VDIS image analysis software and the mean CIELAB and WIO of the upper central incisors will be obtained.

Study Design

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

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Two upper central incisors must be natural.
  • The two upper central incisors must be within the colours of 2M2, 3R1.5, 2R2.5, 3L1.5, 2L2.5, 4M1, 2M3, 3M2, 4R1.5, 4L1.5, 3L2.5, 3R2.5, 5M1, 4M2, 3M3 from VITA 3D-MASTER Shade Guide.
  • The two upper central incisors must be free of intrinsic stain e.g. caused by tetracycline, fluorosis etc.
  • The two upper central incisors must be extrinsic stain free.
  • Willing to sign an informed consent form and complete a medical history questionnaire.

Exclusion Criteria

  • Two upper central incisors have any caps, crowns, veneers or cracks in the teeth, have excessive gum recession, or have restorations on the distal, mesial, buccal, incisor edge in the opinion of the dentist and technician.
  • Smoker (including e-cigarettes) or chews tobacco.
  • Are diabetic
  • Currently pregnant or breast feeding.
  • Currently having orthodontics bands, partial removable dentures.
  • Currently experiencing severe oral problems such as untreated caries, gingivitis or periodontal disease.
  • Regular use of medication, which in the opinion of the study dentist, could interfere with study objectives.
  • Known allergies to the toothpaste ingredients or to any dental materials.
  • Use of tooth bleaching products in the past 6 months.
  • Have been using whitening oral care products in the last 12 weeks or had a scale and polish in the last 3 months.
  • Have or have had a medical condition that in the opinion of the study dentist would make them unsuitable for inclusion.

Arms & Interventions

Test toothpaste 2

Experimental

Silica-based toothpaste containing blue covarine and fluoride as sodium monofluorophosphate

Intervention: Silica-based fluoride toothpaste with blue covarine (Other)

Test toothpaste 1

Experimental

Silica-based toothpaste containing charcoal, clay, blue covarine, green covarine and fluoride as sodium fluoride

Intervention: Silica-based fluoride toothpaste containing clay, charcoal, blue covarine and green covarine (Other)

Test toothpaste 3

Experimental

Silica-based toothpaste containing blue covarine and fluoride as sodium monofluorophosphate

Intervention: Silica-based fluoride toothpaste with blue covarine (Other)

Control toothpaste

Other

Control silica-based toothpaste containing fluoride as sodium fluoride

Intervention: Control silica-based fluoride toothpaste (Other)

Outcomes

Primary Outcomes

Tooth whiteness index (WIO) (average value from two upper central incisors

Time Frame: Immediately after brushing

Digital images of the upper central incisors will be taken before and immediately after brushing with toothpaste using a Video-based Digital Imaging System (VDIS). WIO will be obtained from VDIS images\[1\]. The outcome measure per participant will be the average values from two upper central incisor teeth. Increase in WIO means whiter. \[1\] Luo, Wen et al. J Dent. 2017;67S:S15-S19.

Secondary Outcomes

  • Tooth Color Lightness L* (average value from two upper central incisors)(Immediately after brushing)
  • Tooth Color a* (red/green) (average value of two upper central incisors)(Immediately after brushing)
  • Tooth Color b* (blue/yellow) (average of two upper central incisors)(Immediately after brushing)

Investigators

Sponsor
Unilever R&D
Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (1)

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