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Clinical research of pain during restorative treatment in adults using a topical anesthetic photoactivated

Clinical investigation of intraoperative pain in adults undergoing restorative treatment of non-carious lesions using a topical anesthetic photoactivated - : Anesthetics; Dental Anxiety; Dental materials

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-6hxhx7
Enrollment
Unknown
Registered
2016-08-15
Start date
2015-03-15
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

Dental caries

Interventions

Treatments not carious V class will be held in cervical premolars of 50 patients. The topical anesthetic photoactivated (experimental group) or photoactivated placebo (control group) to be used will b
1 = mild pain
2 = moderate pain
3 = severe pain, 4 = unbearable pain) in which the patient will report their pain. The intervention will be performed first in quadrant 1 when superior arch or quadrant 3 if lower arch. After isolatio
Other
E06.323.428

Sponsors

Universidade Estadual de Ponta Grossa
Lead Sponsor
Universidade Estadual de Ponta Grossa
Collaborator

Eligibility

Age
18 Years to 80 Years

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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.

Countries

Brazil

Contacts

Public ContactAlessandra Reis

Universidade Estadual de Ponta Grossa

reis_ale@hotmail.com+55 (42) 3220 3741

Outcome results

None listed

Source: REBEC (via WHO ICTRP)