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Study of the therapies for dentin hypersensitivity.

Comparative study of therapies for the treatment of non-carious cervical lesions with dentinal hypersensitivity

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-4x2957
Enrollment
Unknown
Registered
2013-08-13
Start date
2012-03-20
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

Tooth wear,Dentine hypersensitivity,Dental Materials

Interventions

Six individuals will be selected with four teeth moderately to severely hypersensitive. In each individual, sensitive teeth will be randomly distributed into the following treatment groups: group 1 (
group 2 (6 teeth) - use of KNO3NaF and immediate restoration with composite resin Filtek Z250 (FZ250)
group 3 ( 6 teeth) – use of KNO3NaF once a week until remission of pain and restoration with FZ250
group 4 ( 6 teeth) - restoration with FZ250. The assessment periods will 0, 7, 30, 90 and 180 days
Procedure/surgery

Sponsors

Universidade Federal do Piauí
Lead Sponsor
Universidade Federal do Piauí
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: The volunteers: they will be included with age 18 years or older, enrolled in the clinics of dentistry UFPI having at least 20 dental elements. Non-carious lesions: at least four lesions whose sensitivity is classified by the patient for moderate to severe after administration of a air, and tooth wear between 2 and 4. These teeth must have an antagonist tooth.

Exclusion criteria

Exclusion criteria: The patient: will be excluded people who have made periodontal treatment and/or hypersensitivity treatment in the last six months, patients with bruxism in the active phase. Non-carious lesions: teeth with very deep lesions, when a ruber dam isolation is not possible and those that have been previously restored.

Design outcomes

Primary

MeasureTime frame
It is expected that one of the interventions is more effective in controlling dentinal hypersensitivity not carious lesions. The outcome will be assessed by analyzing the presence of pain induce by an air jet against the site where the intervention was carried out.

Secondary

MeasureTime frame
It is expected that all interventions are effective up to 6 months of intervention.

Countries

Brazil

Contacts

Public ContactRaimundo Prado Júnior

Universidade Federal do Piauí

rosendo_prado@ig.com.br(86)32155888

Outcome results

None listed

Source: REBEC (via WHO ICTRP)