Dental Assistants
Conditions
Interventions
Open-label, randomized controlled trial on demand acetaminophen prescription. Patients in need of clinical crown augmentation were included in the study. After surgery, the patient was allocated to th
Drug
Procedure/surgery
V03.175.250.500.500
Sponsors
Universidade Federal do Rio Grande do Sul
Faculdade de Odontologia UFRGS
Eligibility
Inclusion criteria
Inclusion criteria: Adult patients; Patients of both sexes; Patients in need of periodontal surgery with total flap to restore supracrystal insertion tissues.
Exclusion criteria
Exclusion criteria: Patients who use systemic analgesics; patients who use systemic antimicrobial, patients who use systemic anti-inflammatory drugs; patients who use systemic muscle relaxants; patients on systemic anxiolytic or antidepressant use; patients with previous chronic or acute pain, related or not to the oral cavity; patients who have difficulty understanding instructions (cognitive changes), impairing the application of the scales proposed by the research.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative pain assessed by the Visual Analog Scale, Numerical Scale and Verbal Pain Scale 2, 6, 12, 24 and 48 hours immediately after surgery. | — |
Secondary
| Measure | Time frame |
|---|---|
| Amount of acetaminophen consumed by the demand group and amount of rescue medication consumed by the test and control groups within 48 hours.;Preoperative anxiety level measured by the IDATE - traço e Estado scales and dental anxiety level measured by the Corah Scale. | — |
Countries
Brazil
Contacts
Public ContactPatricia Weidlich
Universidade Federal do Rio Grande do Sul
Outcome results
None listed