Comparative evaluation of the effects of different anesthesia techniques on the patients'
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Having molar incisor hypomineralization, no comprehension or speech problems and being willing to participate in the study, 2) The legal representative's child being willing to participate in the study and his/her consent being obtained, 3) Not having a systemic disease that would constitute a contraindication for dental treatment or anesthesia and not using regular medication, 4) The patient group not having any physical or physical disabilities, 5) Not having any hereditary or acquired diseases or syndromic conditions, 6) Not having had any previous dental treatment, 7) Having active caries that did not exceed 1/3 of the dentin in the mandibular right or left first molar teeth, 8) Teeth requiring Class II cavity preparation, 9) Not having a history of acute pain
Exclusion criteria
Exclusion criteria: 1) Children with no molar hypomineralization, who do not volunteer to participate in the study, who have the potential to harm others, who cannot do their own work, understand, make decisions, speak due to mental weakness, or who require constant assistance for their protection and care, 2) Children whose legal representatives do not volunteer for their children to participate in the study and whose consent cannot be obtained, 3) Children who do not sign the informed consent form and their legal representatives, 4) Patients with systemic diseases and regular medication use, 5) Patients with irreversible pulpitis, cellulitis findings and acute pain, 6) Teeth with caries exceeding 1/3 of the dentin, teeth with indications for amputation and root canal treatment, 7) Syndromic individuals with hereditary and acquired diseases, 8) Those who have previously had any trauma to their teeth to be treated, 9) Patients who report an allergy to local anesthetic drugs, 10) Patients in the definitely negative group according to the Frankl behavior scale
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain Before and after anesthesia Scale and salivary opiorphin value | — |
Secondary
| Measure | Time frame |
|---|---|
| Anxiety Before and after anesthesia Scale and salivary opiorphin value | — |
Countries
Turkey
Contacts
Faculty of Dentistry, Mersin University