Unspecified obesity
Conditions
Interventions
Sponsors
Plinio da Cunha Leal
Universidade Federal de São Paulo
Eligibility
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Age between 18 and 65 years; both sexes; American Society of Anesthesiologists (ASA) physical status I, II, or III; patients undergoing Sleeve type bariatric surgery
Exclusion criteria
Exclusion criteria: Severe comorbidity with American Society of Anesthesiologists (ASA) physical status IV; cardiac arrhythmias; dilated cardiomyopathy; cardiac conduction disturbance; electrolyte disturbance; acid-base disturbance; hypersensitivity to lidocaine; psychiatric, hepatic, respiratory or oncological diseases, who are receiving any type of analgesic in the week before surgery; patients receiving hemoderivatives during the study period
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find less postoperative pain according to the visual analog scale in the patients of the intervention group | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate postoperative opioid consumption between the groups;To compare the quality of post-anesthesia recovery between the groups studied by applying validated questionnaires | — |
Countries
Brazil
Contacts
Public ContactPlinio Leal
Hospital São Domingos
Outcome results
None listed