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Evaluation of Adhesive for Children's Mouth Anesthesia

Evaluation of the Efficacy of a Non-Invasive Anesthetic Polymeric Device - Randomized Clinical Trial in Children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-42chrz
Enrollment
Unknown
Registered
2018-10-30
Start date
2018-05-08
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

Stomatognathic Diseases Dental cavity Tooth Avulsion Deciduous Tooth

Interventions

We will select 50 children who are being treated at the Pediatric Dentistry Clinic of FORP USP, who need to perform procedures such as sealants, restorations and extraction in teeth with more than 2/3
Drug
Device
Behavioural
E03.091

Sponsors

Faculdade de Odontologia de Ribeirão Preto
Lead Sponsor
Faculdade de Odontologia de Ribeirão Preto
Collaborator

Eligibility

Age
4 Years to 12 Years

Inclusion criteria

Inclusion criteria: Children of both sexes; from four to twelve years; healthy; which have at least two homologous and contralateral teeth in the upper arch; with indication of similar dental procedures. Teeth requiring local anesthesia in routine clinical treatment.

Exclusion criteria

Exclusion criteria: Children with contraindications to the use of local anesthetics; with cognitive impairments; teeth that need treatment like pulpotomy; endodontic treatment; extraction of teeth with more than two thirds of the root; deep cavity restorations.

Design outcomes

Primary

MeasureTime frame
It is expected that the children served by the study using the anesthetic device do not require anesthesia complementation, evidenced by the absence of painful symptomatology during the clinical procedures.

Secondary

MeasureTime frame
Secondary outcomes are not expected.

Countries

Brazil

Contacts

Public ContactAlexandra Queiroz

Faculdade de Odontologia de Ribeirão Preto

amqueiroz@forp.usp.br+55-16-33153995

Outcome results

None listed

Source: REBEC (via WHO ICTRP)