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Not yet recruitingNCT05789004Updated Nov 4, 2024

Efficacy of Tooth Bleaching With 35% and 6% Hydrogen Peroxide in Primary Dentition

A Phase 1/2 interventional study of Tooth Bleaching with Whiteness HP Automixx 35% and Tooth Bleaching with Whiteness HP Automixx 6% in Sensitivity, Tooth, sponsored by University of Nove de Julho. Not yet recruiting. Open to participants aged 3 Years to 6 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-11-04.

Sponsored by University of Nove de Julho · Phase 1/2, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Aug 2025, 1 year 2 months ago, but the record still lists the study as not yet recruiting.
Phase
Phase 1/2
Study type
Interventional
Enrollment
38
Allocation
Randomized
Ages
3 Years to 6 Years
Sex
All
01

Study summary

The aesthetics of dental elements generates great psychological and social impacts, both in the deciduous and permanent dentition. One of the techniques widely used to visually improve the appearance of teeth is bleaching. Bleaching can be performed both at home and in a dental office. In office whitening, the technique used consists of applying the whitening gel to the dental surfaces in concentrations ranging from 25% to 50% of hydrogen peroxide. However, recent studies show that low and medium concentration bleaching agents based on hydrogen peroxide have been effective and present a lower risk of sensitivity to the patient. In view of the above, this study aims to carry out a controlled and randomized clinical trial to compare the effectiveness of dental bleaching in deciduous teeth with hydrogen peroxide at concentrations of 35% and 6%. For this, 38 patients aged 03 to 06 years will be selected, allocated in 2 groups (G1 - Hydrogen Peroxide 35%, n=19 and G2- Hydrogen Peroxide 6%, n=19). Bleaching will be carried out in up to three sessions, with an interval of 7 days between them and the evaluation of color and tooth sensitivity will be carried out 48 hours after each bleaching session. The color assessment will be measured using a digital spectrometer and tooth sensitivity using the Pain Level Scale (Wong-Baker Faces®). Descriptive statistical analysis will be carried out, containing the mean and standard deviation in the calculation and normality and homogeneity tests will be carried out, for subsequent adequate statistical analysis. As a result, it is expected that there is no significant difference between the groups in terms of color variation and that the low-concentration bleaching group has the lowest sensitivity index.

02

Conditions studied

  • Sensitivity, Tooth

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03

In context

Dentin Sensitivity

288 studies on the registry are indexed under Dentin Sensitivity; 46 are open to participants now.

This study's planned enrollment of 38 is below the median of 60 across 279 interventional studies indexed under Dentin Sensitivity.

Browse Dentin Sensitivity studies →

Lead sponsor

University of Nove de Julho is the lead sponsor of 246 studies on the registry; 52 are open to participants now.

Of its 8 completed or terminated interventional studies of FDA-regulated products, 1 (13%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
3 Years to 6 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age range from 03 to 06 years old;
  • Vital or non-vital teeth (already endodontically treated) with severe to moderate discoloration;
  • No active carious lesions;
  • No lesions in the oral cavity;
  • No report of previous tooth sensitivity.

Exclusion criteria

Exclusion Criteria:

  • Patients who during anamnesis report allergies to dyes or latex, who withdraw from participating in the study, as well as those who do not attend the callbacks, will be excluded.
05

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
38 participants (estimated)

Study arms

  • Experimental
    Hydrogen Peroxide 35%

    In the participants of this group, the tooth whitening process will be performed with 35% hydrogen peroxide.

    Procedure: Tooth Bleaching with Whiteness HP Automixx 35%

  • Experimental
    Hydrogen Peroxide 6%

    In the participants of this group, the tooth whitening process will be performed with 6% hydrogen peroxide.

    Procedure: Tooth Bleaching with Whiteness HP Automixx 6%

Interventions

  • ProcedureTooth Bleaching with Whiteness HP Automixx 35%

    * Clinical examination and taking the initial shade of the tooth with Vita Easyshade®; * Sensitivity/pain recording using the Pain Level Scale (Wong-Baker Faces®); * Prophylaxis with a Robson brush and prophylactic paste; * Application of lip balm on the patient's lips; * Placement of the labial retractor; * Application of the gingival barrier; * Application of Whiteness HP Automixx 35% whitening gel; * In the session, a single application of the gel will be carried out and where it will remain on the surface of the tooth for 15 min; * The gel must be removed from the teeth with a sucker and the teeth cleaned with gauze; * Sensitivity/pain recording using the Pain Level Scale (Wong-Baker Faces®); * The second bleaching session will be carried out 7 days after the first one and, if necessary, a third session can be carried out 7 days after the second one.

  • ProcedureTooth Bleaching with Whiteness HP Automixx 6%

    * Clinical examination and taking the initial shade of the tooth with Vita Easyshade®; * Sensitivity/pain recording using the Pain Level Scale (Wong-Baker Faces®); * Prophylaxis with a Robson brush and prophylactic paste; * Application of lip balm on the patient's lips; * Placement of the labial retractor; * Application of the gingival barrier; * Application of Whiteness HP Automixx 6% whitening gel; * In the session, a single application of the gel will be carried out and where it will remain on the surface of the tooth for 15 min; * The gel must be removed from the teeth with a sucker and the teeth cleaned with gauze; * Sensitivity/pain recording using the Pain Level Scale (Wong-Baker Faces®); * The second bleaching session will be carried out 7 days after the first one and, if necessary, a third session can be carried out 7 days after the second one.

06

What researchers measure

Primary outcomes

  1. Changes in tooth color

    The Vita Easyshade® digital spectrometer (VITA Zahnfabrik H. Rauter GmbH \& Co. KG, Germany) will be used for evaluation. The upper left canine will be used as a color reference because it is the most saturated tooth in the arch (greater dentin mass and greater amount of intrinsic pigments).

    Time frame: Baseline and 48 hours after each bleaching session.

  2. Changes in tooth sensitivity

    It will be explained to the participant that each face drawn in a figure represents a person who has no pain, or some, or a lot of pain. Face 0 doesn't hurt at all. Face 2 hurts a little. Face 4 hurts a little more. Face 6 hurts a lot. Face 8 hurts the most. Face 10 hurts as much as you can imagine, although you don't have to be crying to have this worst pain. The participant will choose the face that best portrays the pain they are experiencing.

    Time frame: Baseline and 48 hours after each bleaching session.

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 4, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05789004
Responsible party
Sandra Kalil Bussadori (Principal Investigator, University of Nove de Julho) — Principal investigator
First posted
Mar 29, 2023
Start date
Mar 1, 2025 (estimated)
Primary completion
Aug 20, 2025 (estimated)
Completion
Mar 20, 2026 (estimated)
Last update
Nov 4, 2024

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2024. You cannot join it, but the record below documents what was studied.

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