Quality of life assessment after dental sensitivity treatment with ozone oil

Not Applicable

• Conditions: Dentin sensitivity; C07.793.266

• Registration Number: RBR-3nqhfy
• Lead Sponsor: FVJM

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-08-17
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Data analysis completed
• Sex: Not specified
• Target Recruitment: Not specified

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

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.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
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<br>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.