Evaluating the effect of using topical anesthesia at the needle insertion and injection site in the labial mucosa of anterior maxilla teeth in terms of time and to compare the effect of dental anxiety Anxiety,
Conditions
Interventions
Anestol was applied to the maxillary anterior for 1 min.
Placebo was applied to the other side of maxilla for 1 min.,Anestol was applied to the maxillary anterior for 3 min.
Placebo was applied to the
Anestol 1 and Control,Anestol 3 and Control,Jetex 1 and Control,Jetex 3 and Control
Sponsors
none
none,none
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Participants had to aged 18–65 years, had ASA I or II category, having able to read and willingness to participate, have no intolerance and/or allergy to the ingredients of the drugs to be used in the study. The patients had to have maxillary teeth to be either root canal or restorative treatment
Exclusion criteria
Exclusion criteria: None of the patients had used sedative analgesics and anxiety medications for the 12 hours prior to the study and there were no pregnant or breastfeeding women.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reducing of injection pain 1 and 3 min VAS scale | — |
Secondary
| Measure | Time frame |
|---|---|
| Measure anxiety level Before treatment MDAS | — |
Countries
Turkey
Contacts
Public ContactFatih Aksoy
Study director
Outcome results
None listed