postoperative pain
Conditions
Interventions
A randomized clinical trial will be carried out, controlled by the prescription of paracetamol (500mg) + codeine (30mg) in a fixed schedule. Thirty-eight adult patients of both sexes will be included
D25.339.312
Sponsors
Faculdade de Odontologia da Universidade Federal do Rio Grande do Sul
Faculdade de Odontologia da Universidade Federal do Rio Grande do Sul
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Adult patients (aged 18 years or older), of both sexes, who need surgery to install at least 3 dental implants or dental implant protocols, with the objective of prosthetic rehabilitation will be included.
Exclusion criteria
Exclusion criteria: Individuals will be excluded: - who present a previous picture of chronic or acute pain, related or not to the oral cavity, - in chronic or acute systemic use (in the 48 hours prior to the procedure) of analgesic, anti-inflammatory and/or muscle relaxant, - with difficulty in understanding instructions (cognitive changes), which impair the application of the scales proposed by the study, such as illiterate patients, with inability to numerically notate and write the pain parameters proposed by the study, - with contraindication for the use of ibuprofen, - with contraindication for the use of paracetamol associated with codeine.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction in the level of postoperative pain by 50% by the use of analgesic in the test group, at 6 hours postoperatively. | — |
Secondary
| Measure | Time frame |
|---|---|
| Reduction in total postoperative facial edema of 5mm in the test group compared to the control group at 48 hours postoperatively. | — |
Countries
Brazil
Contacts
Public ContactPatricia Weidlich
Universidade Federal do Rio Grande do Sul
Outcome results
None listed