Clinical Trials in Brazil / NCT07597044
Active, not recruiting Not applicable

Evaluation of Sensitivity and Color Change of Different Protocols of In-office Dental Bleaching

NCT07597044 · tracked via the Priya Life Science Brazil tracker
Phase
Not applicable
Started
2025-10-01
Last updated
2026-05-19

Condition(s) studied

Tooth Sensitivity

Investigational drug(s) / intervention(s)

Standard in-office tooth bleachingAlternative in-office tooth bleaching

Standard in-office tooth bleaching: Patients will have their teeth bleached in-office using 40% Hydrogen Peroxide (commercial available product - Opalescence Boost, Ultradent Products International) in two sections with 7 days of interval between sections. In each section, the product will be used during 40 minutes according to manufacturer's instructions.

Alternative in-office tooth bleaching: Patients will have their teeth bleached in-office using 40% Hydrogen Peroxide (commercial available product - Opalescence Boost, Ultradent Products International) in two sections with 7 days of interval between sections. In each section, the product will be used during 20 minutes, will be removed with water, and another application of 20 minutes will be made.

Study summary

Clinical randomized single-blind trial, used to measure the level of tooth sensitivity (TS) after in-office dental bleaching sessions, on volunteers using a modified visual analog scale (VAS). The investigators selected for this study, 40 participants with color 2M2 or darker (Using OM1 - 5M3 Vita bleaching shade guide). The investigators performed two bleaching sessions with a 40% hydrogen peroxide gel with a 1-week interval. Participants were enrolled in two groups. In one group, the bleaching product was used according to manufacturer's instructions (40-minutes application in each section). In the other group, the bleaching product was used in two 20-minutes applications in each section.The investigators recorded the TS up to 48h with a VAS scale and the color at baseline and 30 days after bleaching with a value-oriented shade guide and a spectrophotometer. The risk and intensity of TS and the color change were compared between the two groups.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * The selected volunteers should: * Present Good general state of health * Be at least 18 years of age * Have an acceptable oral hygiene * Present the upper and lower arches without absence of teeth of first premolar right to the left first premolar. * Have anterior teeth with any kind of restoration. * Be No smoker * Have the upper right canine with color 2M2 or darker Exclusion Criteria: * The selected volunteers should not: * Have medical history of diseases that can affect the results of the study * Have made use of cigarettes in the last 30 days * Have some important pathology in the oral cavity * Be pregnant * Be breastfeeding * Have moderate advanced periodontal disease; * Have consumed drugs, alcool or any medication that can cover the results, as other types of anti-inflammatories or painkillers; * Have used products indicated for dental sensitivity, as desensitizing toothpaste or similar product * Present gingival recession * Present exacerbated hypersensitivity history

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Universidade Federal Fluminense - School of Dentistry Nova Friburgo Rio de Janeiro

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07597044 on ClinicalTrials.gov ↗ ← All trials in Brazil