Periodontal disease
Conditions
Interventions
Dental surface anesthesia using Anespatch or Anespatch no needle before local anesthesia
Sponsors
Kiriishi Kensuke
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.Patients who visited the dental department of Nagasaki University Hospital and were diagnosed as needing SRP under infiltration anesthesia for periodontal disease in the maxillary premolar area on both sides 2.Patients with remaining maxillary premolars on both sides 3.Age: Adult patients aged 18 to 85 years at the time of obtaining consent 4.Any gender 5.Inpatient/outpatient: Outpatient only 6.Patients who have received a sufficient explanation of their participation in this study, fully understood the study, and voluntarily provided written consent
Exclusion criteria
Exclusion criteria: 1.Patients who regularly use analgesics 2.Patients with a history of hypersensitivity to benzoate ester-based local anesthetics 3.Patients with methemoglobinemia 4.Pregnant and breastfeeding women 5.Patients who the principal investigator deems inappropriate to be study subjects
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Degree of pain during local anesthesia(VAS) | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Depth of surface anesthesia 2.Blood pressure, pulse rate, and transcutaneous oxygen saturation before and after patch application at 5-minute intervals 3.Discomfort caused by the Anes patch | — |
Contacts
Public ContactKensuke Kiriishi
Nagasaki University Hospital
Outcome results
None listed