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The effect of Activated Carbon-Based Toothpastes: Randomized clinical study

Efficacy of Activated Carbon-Based Whitening Dentifrices: Randomized clinical study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-10nwcpsx
Enrollment
Unknown
Registered
2021-05-31
Start date
2021-08-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fluorosis, Dental

Interventions

This is a single-blind study, only the evaluators will be blinded due to the characteristics of the materials tested. The randomization will be performed on the website www.sealedenvelope.com by a res
The teeth will be rinsed under running water
After that, the teeth will be brushed with a conventional toothpaste, for 90 seconds
Protocol repeated three times a day for 14 days, after that time the product will be used only twice a week. They will be instructed to use dental floss, but not to use mouthwash. G2, group activated
Protocol repeated three times a day for 14 days. They will be instructed to put a pea-sized amount of toothpaste, use dental floss, but do not use mouthwash. G4, 10% carbamide perox
SP4.606.713.156.276
D25.37

Sponsors

Universidade do Norte do Paraná
Lead Sponsor
Universidade do Norte do Paraná
Collaborator

Eligibility

Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 18 to 40 years old and in good general health; six upper teeth fully erupted; without oral disease or dental restorations; at least one upper tooth showing A3 or darker shade, as measured with Vita Easyshade Advance 4.0 (Vita Zahnfabrik, Bad Säckingen, Germany) (ordered by brightness).

Exclusion criteria

Exclusion criteria: Systemic diseases or disorders of the oral mucosa; pre-lightening treatments; current orthodontic treatment or with parafunctional habits; pregnancy or lactating; known allergies to the product's ingredients; smoke; alcohol abuse; gingival recession; with structural enamel defect or with a history of dentin hypersensitivity; with one of the six anterior teeth with caries or a non-carious cervical lesion; with one of the six anterior teeth with more than 1/6 of its buccal surface restored; with one of the six anterior teeth with a medium shade lighter than A2.

Design outcomes

Primary

MeasureTime frame
Expected outcome 1: To evaluate the bleaching efficacy, using the Vita Classical, Vita Bleachedguide (?SGU) and VitaEasyshade spectrophotometer (?Eab, ?E00 and ?WID) scales of volunteers submitted to different treatments (activated charcoal powder, activated charcoal toothpaste, conventional toothpaste and 10% carbamide peroxide). It is expected that whitening efficacy will depend on the treatment performed.;Outcome found 1: Activated charcoal products have no significant effect on color change when compared to 10% carbamide peroxide.

Secondary

MeasureTime frame
Expected outcome 2: The intensity of dental sensitivity will be evaluated using the VAS analogue visual scale (0-10). It is expected that sensitivity will depend on the treatment performed.;Outcome found 2: No significant difference was found among the groups regarding to sensibility intensity.;Expected outcome 3: To assess the acceptability of the treatments carried out by the research participants. Acceptability is expected to depend on the treatment performed.;Outcome found 3: Activated charcoal-based products are less acceptable than 10% carbamide peroxide.;Expected outcome 4: The effect on enamel roughness will be evaluated by means of replicates and the effect will be according to the treatment performed.;Outcome found 4: Products based on activated charcoal promote an increase in the roughness of dental enamel, regardless of presentation form (powder or toothpaste). ;Expected outcome 5: Significant differences in the impact of oral health on quality of life are expected depending on the treatment, using the Oral Health Impact Profile-14 questionnaire (OHIP-Esthetics) and the Psychosocial Impact of Dental Aesthetics Questionnaire (PIDAQ);Expected outcome 6: To evaluate the aesthetic self-perception, using the Orofacial Aesthetics Scale (OAS) of volunteers submitted to protocols (activated charcoal powder, activated charcoal toothpaste, conventional toothpaste and 10% carbamide peroxide).;Outcome found 6: OES questionnaire, significant increase only in the tooth color domain for the 10% carbamide peroxide.

Countries

Brazil

Contacts

Public ContactAndrey Emidio

Universidade do Norte do Paraná

andrey.goncalves130@gmail.com+55(044)999150363

Outcome results

None listed

Source: REBEC (via WHO ICTRP)