Dental Anxiety
Conditions
Interventions
This is a two-arm, single-blind, randomized controlled clinical study. A total of 80 people who meet the eligibility criteria will be probabilistically allocated to groups intervention and control usi
control group and intervention group. Firstly, participants will sign an Informed Consent Form (TCLE) and, after acceptance, they will respond to a questionnaire with sociodemographic data collection.
E03.155.086.231
Sponsors
Editora e Distribuidora Educacional S/A
Faculdade Anhanguera de Rondonópolis (FAR)
Eligibility
Age
20 Years to 45 Years
Inclusion criteria
Inclusion criteria: Healthy volunteers; both genders; non-smokers; age range between 20 and 45 years; in need of jaw extraction; signature on the free and informed consent form
Exclusion criteria
Exclusion criteria: Patients who use anxiolytics; uncontrolled systemic diseases; history of alcohol or drug abuse and patients who withdraw from the study at any time or who do not sign the Informed Consent Form
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is hoped that local anesthesia prior to setting up the fields will be a method capable of reducing anxiety by 15%, which may lead to fewer changes in vital signs and a better anesthetic effect of vasoconstriction | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes expected | — |
Countries
Brazil
Contacts
Public ContactRodrigo de Barros
Universidade de Cuiabá UNIC
Outcome results
None listed