postoperative pain
Conditions
Interventions
Control group: 35 patients will receive standard analgesia from the study institution, according to medical prescription time, during the first postoperative dressing of tibial fracture surgery.
Exper
Drug
Other
E02.190.888.500
E03.091
Sponsors
Universidade Federal de Sergipe
Universidade Federal de Sergipe
Eligibility
Age
18 Years to 59 Years
Inclusion criteria
Inclusion criteria: Patients aged 18 years and over and under 60; immediate postoperative period of surgical treatment of exposed tibial fracture and submitted to spinal anesthesia; who had no associated fractures; who had not been on central nervous system depressant drugs for 12 hours; had no reports of allergy to standard institution analgesia.
Exclusion criteria
Exclusion criteria: Present a history of chronic pain; impaired verbal communication; altered hearing acuity; dislike music or that it does not bring good feelings; those who were using another non-pharmacological pain relief method or did not understand pain assessment tools.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain, determined by means of its intensity assessment tools, the Visual Numerical Scale (EVN) and the Revised Facial Pain Scale (EFD-R), before and after the first postoperative tibial fracture dressing | — |
Secondary
| Measure | Time frame |
|---|---|
| No Secondary Outcomes Expected | — |
Countries
Brazil
Contacts
Public ContactMaria Leite Ferraz
Universidade Federal de Sergipe
Outcome results
None listed