Dental Anesthesiology
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients undergoing dental treatment requiring local anesthesia
Exclusion criteria
Exclusion criteria: Severe cardiovascular disease (unstable angina, myocardial infarction within the past 6 months, severe heart failure (NYHA class III/IV), severe arrhythmia) Blood pressure-related disorders (secondary hypertension, severe hypertension ) Drug-related (Contraindications to epinephrine-containing lidocaine hydrochloride preparations, use of beta-blockers) Pharmacologically assisted behavioral modification (Psychotropic sedation, general anesthesia) Other (Pregnancy or lactation, contraindications to upper arm blood pressure measurement, difficulty cooperating due to dementia, psychiatric disorders, intellectual disability, etc. Deemed inappropriate by the principal investigator)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Blood pressure and pulse rate after local anesthesia: Measure and record blood pressure and pulse rate twice each immediately before, immediately after, 5 minutes after, 10 minutes after, and 30 minutes after the local anesthetic injection. Compare the change rate in systolic blood pressure between the white coat effect group and the control group. Furthermore, the primary endpoint was a multivariate linear regression analysis adjusted for age, sex, BMI, medical history, epinephrine dose, and treatment content. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints include the change rate in diastolic blood pressure, change rate in mean arterial pressure, change rate in heart rate, and incidence rate of adverse events. | — |
Countries
Japan
Contacts
Kanagawa Dental University Department of Anesthesiology, Division of Dental Anesthesiology