Clinical research of pain during restorative treatment in adults using a topical anesthetic photoactivated
Not Applicable
- Conditions
- Dental cariesDental Restoration FailureAnesthesia, DentalDentin SensitivityC07.793.720.210E06.323.400E03.155.141C07.793.266
- Registration Number
- RBR-6hxhx7
- Lead Sponsor
- niversidade Estadual de Ponta Grossa
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruitment completed
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Patients over 18 years; with good general and oral health; the premolar teeth should have restorative treatment indication not carious cervical; these non-carious lesions should involve two teeth in different quadrants.
Exclusion Criteria
Endodontically treated teeth; destroyed and caries; also excluded are patients with gingivitis; periodontitis and dental mobility; in addition, patients with a history of allergy; any form of sensitivity or allergic reaction to anesthetics and ester-based components of the formula; patients with severe uncontrolled systemic disease (heart problems; neurological; kidney; liver or blood); pregnant or lactating patients.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Expected outcome: Number of patients reporting pain during the placement of a staple for absolute isolation after application of a topical anesthetic photoactivated through self-report. This number will be transformed into percentage of patients with pain and is called absolute risk of pain.
- Secondary Outcome Measures
Name Time Method Expected outcome: The intensity of the pain will be assessed using a scale of 5 points (NRS 0-4) and visual analogue scale VAS (0-100) and will be presented as mean and standard deviation.;Expected outcome: The pain of the risk will be assessed by dichotomous scale (yes or no) and will be presented as mean and standard deviation.