Obesity
Conditions
Interventions
All patients will receive intravenous general anesthesia with propofol 2 mg.kg-1, fentanyl 3 mcg.kg-1, dexmedetomidine 0.5 mcg.kg-1 and rocuronium (dose depending on randomization). Intraoperatively,
Sponsors
Hospital São Domingos
Hospital São Domingos
Eligibility
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: aged between 18 and 65 years, both sexes, with an ASA score from 1 to 3, undergoing roux-en-y gastric bypass by robotic surgery will be included in the study.
Exclusion criteria
Exclusion criteria: Patients with cardiac arrhythmias, dilated cardiomyopathy, cardiac conduction disorder, electrolyte disturbance, acid base disturbance, known or suspected allergies to drugs used during anesthesia, family history of neuromuscular disease, family history of malignant hyperthermia, and renal failure, psychiatric, hepatic, respiratory or oncological diseases, who are receiving any type of analgesic in the week before surgery and those who receive blood products during the study period.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Patients in the sustained deep neuromuscular blockade group are expected to obtain better surgical conditions with reduced postoperative pain and consequently lower postoperative pain scores. Assessment will be performed using questionnaires at defined times to check pain intensity, time of first request for opioid use and total opioid consumption in the first 24 hours. | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary results expected | — |
Countries
Brazil
Contacts
Public ContactHiago Parreão Braga Braga
Hospital São Domingos
Outcome results
None listed