- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03760367
Investigation of the Instant Tooth Whitening Effect of a Silica Toothpaste Containing Blue Covarine
Investigation of the Instant Tooth Whitening Effect of a Silica Toothpaste Containing Blue Covarine - a Randomized Controlled Clinical Trial
The study investigates the effect of toothbrushing with a toothpaste containing blue covarine compared to a control toothpaste without blue covarine on tooth color. Participants brush their teeth once with either the blue covarine containing toothpaste or a control toothpaste for two minutes. Before and after brushing, tooth color is assessed with a spectrophotometer. Moreover, satisfaction of the participants with their tooth color is assessed using a numeric analogue scale before and after treatment.
The null hypotheses are that neither brushing with the toothpaste containing blue covarine nor brushing with the control toothpaste change a) the tooth color and b) the satisfaction of the participants with their tooth color.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Participants are recruited by advertizing in several public areas in Aarhus, Denmark.
Written and oral information on the study is provided, eligibility criteria are checked, and informed consent is given by the participants.
The upper front teeth of the participants are cleaned with pumice and a rubber cup by operator A.
Participants look at the color of their upper front teeth with a mirror, in a room with controlled lighting conditions.
Thereafter, participants rate their satisfaction with the color of their teeth using an 11-point aesthetic numeric analogue scale.
Tooth color is assessed by operator B using a spectrophotometer (VITA Easyshade Advance) and a positioning device to standardize measurements. Measurements are performed in a room with controlled lighting conditions. VITA SYSTEM 3D-MASTER color, L*, a* and b* are recorded.
Participants are then randomly assigned to either the blue covarine toothpaste group or the control toothpaste group.
They are given a short video introduction to the Bass toothbrushing technique by operator C (caregiver).
Operator C provides a toothbrush and 1 g of either blue covarine toothpaste or control toothpaste, according to the randomization scheme.
Participants brush their teeth for two min, starting with the upper front teeth, and then rinse their mouth with tap water.
Thereafter, participants look again at the color of their upper front teeth with a mirror, in the same room as before treatment.
They rate their satisfaction with the color of their teeth using the 11-point aesthetic numeric analogue scale.
Moreover, they rate the color difference before and after treatment on an 11-point aesthetic numeric analogue scale.
Again, tooth color is assessed by operator B using a spectrophotometer (VITA Easyshade Advance) and a positioning device to standardize measurements. Measurements are performed in the room with controlled lighting conditions. Again VITA SYSTEM 3D-MASTER color, L*, a* and b* are recorded.
The null hypotheses of the study are that neither brushing with the toothpaste containing blue covarine nor brushing with the control toothpaste change a) the tooth color and b) the satisfaction of the participants with their tooth color.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Aarhus, Denmark, 8000
- Aarhus University, Department of Dentistry and Oral Health
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Healthy volunteers
Exclusion Criteria:
- Dental caries in the upper front teeth
- Intrinsic stain of the upper front teeth, including tetracyclin stains, fluorosis, and staining due to pulpitis or pulp necrosis
- Dental restorations in the upper front teeth, including fillings, veneers, crowns, and root canal fillings
- Dental anomalies of the upper front teeth, including molar incisor hypomineralisation, amelogenesis imperfecta, and dentinogenesis imperfecta
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Blue Covarine Toothpaste
After a short video introduction to the bass technique, participants brush their teeth once with a silica toothpaste containing blue covarine (Pepsodent White Now Gold, 1 g) for 2 min, starting with the upper front teeth.
Thereafter, participants rinse their mouth with of tap water.
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2 min toothbrushing with 1 g of Pepsodent White Now Gold
Other Names:
|
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Active Comparator: Control Toothpaste
After a short video introduction to the bass technique, participants brush their teeth once with a silica toothpaste (Colgate Advanced Whitening, 1 g) for 2 min, starting with the upper front teeth.
Thereafter, participants rinse their mouth with of tap water.
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2 min toothbrushing with 1 g of Colgate Advanced Whitening
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
3D VITA SYSTEM 3D-MASTER tooth color change
Time Frame: Tooth color is measured twice, right before (baseline) and immediately after toothbrushing.
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Tooth color change of the upper right first incisor is assessed after toothbrushing compared to baseline using a spectrophotometer.
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Tooth color is measured twice, right before (baseline) and immediately after toothbrushing.
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Change of participant satisfaction with the tooth color
Time Frame: Participant satisfaction is assessed twice, right before (baseline) and immediately after toothbrushing.
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Change of participant satisfaction with the color of their upper front teeth is assessed after toothbrushing compared to baseline using an 11 step aesthetic numeric analogue scale (ANA scale, Funk et al., 2011; DOI: https://doi.org/10.1016/j.jcms.2011.07.018).
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Participant satisfaction is assessed twice, right before (baseline) and immediately after toothbrushing.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change of blue-yellow color component of the tooth (b* in the CIELAB color space)
Time Frame: The blue-yellow color component is assessed twice, right before (baseline) and immediately after toothbrushing.
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The change of the blue-yellow color component of the upper right first incisor is assessed after toothbrushing compared to baseline using a spectrophotometer.
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The blue-yellow color component is assessed twice, right before (baseline) and immediately after toothbrushing.
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Change of the green-red color component of the tooth (a* in the CIELAB color space)
Time Frame: The green-red color component is assessed twice, right before (baseline) and immediately after toothbrushing.
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The change of the green-red color component of the upper right first incisor is assessed after toothbrushing compared to baseline using a spectrophotometer.
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The green-red color component is assessed twice, right before (baseline) and immediately after toothbrushing.
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Change of the tooth lightness value (L* in the CIELAB color space)
Time Frame: The tooth lightness is assessed twice, right before (baseline) and immediately after toothbrushing.
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The change of lightness of the upper right first incisor is assessed after toothbrushing compared to baseline using a spectrophotometer.
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The tooth lightness is assessed twice, right before (baseline) and immediately after toothbrushing.
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Participant evaluation of tooth color change
Time Frame: The color change of the upper front teeth is assessed once: immediately after toothbrushing.
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The color change of their upper front teeth is assessed visually by the participants using an 11 step aesthetic numeric analogue scale (ANA scale, Funk et al., 2011; DOI: https://doi.org/10.1016/j.jcms.2011.07.018).
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The color change of the upper front teeth is assessed once: immediately after toothbrushing.
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sebastian Schlafer, Dr., Aarhus University, Department of Dentistry and Oral Health
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- IOOS_TA_01_2018
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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