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Use of in-office bleaching agents with different pH in combined bleaching, a randomized clinical trial

Combined bleaching using in-office bleaching agents with pHs different: a randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-10chb63w
Enrollment
Unknown
Registered
2023-05-29
Start date
2023-06-10
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

Dentin Sensivity

Interventions

At the time of screening, those who fit the profile of the clinical study will have their upper and lower arches molded with alginate and cast with stone plaster. The models will be cut to make indivi

Sponsors

Universidade Ceuma
Lead Sponsor
Universidade Ceuma
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Healthy volunteers; both genders; minimum age of 18 years and maximum without limit; non smokers; have vital teeth free of carious lesions; non-carious in the anterior region; free from periodontal disease; and the upper right canine should be A2 or darker in color compared to the Vita Classical scale; patients must sign the Informed Consent Form after explaining the details of the research

Exclusion criteria

Exclusion criteria: Volunteers with previous tooth sensitivity; who never performed any type of dental bleaching; smokers, pregnant or breastfeeding women; in continuous use of medications such as analgesics or anti-inflammatories; who do not use prostheses; no restorations on the upper anterior teeth; are not using fixed orthodontic appliance; without any parafunction; no gingival recession; no endodontic treatment of anterior teeth, no severe dental discoloration (tetracycline staining or fluorosis) and visible cracks in teeth

Design outcomes

Primary

MeasureTime frame
The will initially assess the absolute risk of tooth sensitivity resulting from professional tooth bleaching when associated with homemade. According to a systematic review of clinical studies that evaluated tooth sensitivity when associated with inpatient tooth bleaching when associated with a trained caretaker, 88% of patients had tooth sensitivity at least once during the whitening procedure. To detect a reduction in the primary outcome from 88% in the control group to 68% in the experimental group, a minimum total of 64 volunteers will be required, with a power of 80% and an alpha of 5%. To contemplate possible follow-up losses, another 16 volunteers per group (25%) will be added, totaling 80 volunteers per group

Secondary

MeasureTime frame
No secondary outcomes expected

Countries

Brazil

Contacts

Public ContactThiago Verde

Universidade Ceuma

thiagocostaverde@hotmail.com+55(98)99223-6448

Outcome results

None listed

Source: REBEC (via WHO ICTRP)