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Evaluation of a bioactive gel to control dental sensitivity in dental bleaching in adolescents

Evaluation of a bioactive gel to control dental sensitivity in dental bleaching in adolescents: double blinded randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-38y9xk6
Enrollment
Unknown
Registered
2025-06-12
Start date
2025-03-24
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 Sensibility, Tooth Bleaching

Interventions

All participants will undergo the same protocol. The procedure begins with dental prophylaxis using pumice and water, followed by the protection of the gingival tissue with a photopolymerizable barrie

Sponsors

Universidade Estadual de Ponta Grossa
Lead Sponsor
Universidade Estadual de Ponta Grossa
Collaborator

Eligibility

Age
12 Years to 16 Years

Inclusion criteria

Inclusion criteria: Good general and oral health (no need for surgery, endodontic, or periodontal treatment); both sexes; age between 12 and 16 years; at least six anterior upper teeth are free of active caries and endodontic treatment; if the anterior teeth have restorations, they must involve no more than 1/3 of the dental structure; canines (13, 23) must be A2 color or darker

Exclusion criteria

Exclusion criteria: Participants are undergoing orthodontic treatment; participants with dental prosthetics; severe tooth discoloration (such as tetracycline stains, fluorosis, or non-vital teeth)

Design outcomes

Primary

MeasureTime frame
Evaluate the dental sensitivity of patients after treatment with bioactive gel

Secondary

MeasureTime frame
Evaluate the effectiveness of the whitening treatment;Evaluate the satisfaction of adolescent patients after whitening treatment

Countries

Brazil

Contacts

Public ContactAna Chibinski

Universidade Estadual de Ponta Grossa

propespsecretaria@uepg.br+55 (42) 3220-3740

Outcome results

None listed

Source: REBEC (via WHO ICTRP)