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Quality of life assessment after dental sensitivity treatment with ozone oil

Quality of life assessment after dentin hypersensitivity treatment with ozone oil - triple blind randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-3nqhfy
Enrollment
Unknown
Registered
2020-08-17
Start date
2019-03-01
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 sensitivity

Interventions

The test group (n = 34) will be submitted to dental hypersensitivity treatment with ozonized oil. The treatment will be applied for 5 minutes to the sensitive area, in a single application. The contr
Procedure/surgery
D26.660

Sponsors

UFVJM
Lead Sponsor

Eligibility

Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients complaining of dentin hypersensitivity with cold, sweets, acidic foods and brushing, and with clinical diagnosis of dentin hypersensitivity; both sexes; without distinction of color or socioeconomic condition; age between 18 to 60 years; with good general and oral health.

Exclusion criteria

Exclusion criteria: Patients presenting restorations and carious lesions in the exposed dentin of hypersensitive teeth; who used painkillers, anti-inflammatories and antidepressants frequently; and, presence of gingival inflammation.

Design outcomes

Primary

MeasureTime frame
Improvement in oral health related quality of life, verified through the DHEQ-15 questionnaire (Dentin Hypersensitivity Experience, 15 items) from the finding of a decrease of at least 10 points in the total score of the questionnaire before and 30 days after intervention.

Secondary

MeasureTime frame
Decrease in the level of dentin hypersensitivity, verified by means of thermal test with ice stick and evaporative test with air jet of the syringe triple, based on the decrease of at least 5% in the pre and post intervention hypersensitivity scores. Reassessments will be carried out immediately and 30 days after treatment.

Countries

Brazil

Contacts

Public ContactDhelfeson Oliveira

UFVJM

dhelfeson@hotmail.com+55 38 35326063

Outcome results

None listed

Source: REBEC (via WHO ICTRP)