Dental Caries
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Both genders; age between 18 and 30 years; any ethnicity; any marital status; any nationality; any place of birth; with previous experience of local anesthesia without intercurrences; not having undergone infiltrative anesthesia in the region in the two weeks prior to the study; and not having used any medication capable of altering pain perception in the two weeks prior to the study
Exclusion criteria
Exclusion criteria: Age lower than 18 years or higher than 30 years old; pregnant or lactating women; history of hypersensitivity to the drugs used in the study; alcohol abuse or drug dependence; psychiatric disorders or systemic diseases; being under treatment with CNS-acting drugs; use of drugs capable of altering pain perception in the two weeks preceding the study; and moderate anxiety or higher (over 9), based on Corah's Dental Anxiety Scale
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome: It is expected to find lower levels of pain during nasopalatine nerve block with the Morpheus® device during puncture, needle insertion and anesthetic deposition, verified by means of the Visual Analog Scale immediately after the anesthetic injection;Obtained outcome: It was observed statistically lower pain levels during nasopalatine nerve block with the Morpheus® device during the puncture, needle introduction, and local anesthetic deposition, verified by means of the Visual Analog Scale immediately after the anesthetic injection | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes are expected | — |
Countries
Brazil
Contacts
Universidade Federal de Sergipe