postoperative pain, Postoperative Nausea and Vomiting
Conditions
Interventions
This is a double-blind randomized controlled clinical study. A total of 50 volunteer participants will be randomly distributed into 2 groups, intervention group with 25 participants and control group
Sponsors
Faculdade de Ciências Médicas de Pernambuco
Complexo Hospitalar do Hospital Universitário Oswaldo Cruz da Universidade de Pernambuco
Eligibility
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Patients of both sexes; candidates for cholecystectomy; no chronic or serious illnesses; with mild or controlled systemic diseases, without functional limitations
Exclusion criteria
Exclusion criteria: Pregnant women; known allergy to the drugs used in the study; bradycardia with a heart rate below 50 bpm; preoperative cardiac conduction block; kidney or liver failure; decompensated psychiatric disorders
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find a reduction in awakening agitation in the intervention group using the Riker scale by at least 50% | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to find a reduction in nausea and pain on the visual scale, in the immediate postoperative period in the intervention group, in a discreet manner. | — |
Countries
Brazil
Contacts
Public ContactIngrid Araújo
Universidade de Pernambuco
Outcome results
None listed