obesity
Conditions
Interventions
Patients in group 1 received lidocaine (1.5 mg / kg) administered for 5 minutes prior to anesthetic induction, and those in group 2, saline solution 0.9% (placebo), in equal volume. Subsequently, veno
Drug
Sponsors
Universidade Federal de São Paulo
Hospital São Domingos
Eligibility
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: age above 18 years; obesity grade 2 or 3; under 65 years
Exclusion criteria
Exclusion criteria: BMI below 35; BMI above 50; children under 18; age over 65 years; allergic to lidocaine
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the time of postoperative ileus after laparoscopic gastric bypass in roux y with perioperative venous lidocaine administration, estimating the reduction in 12 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the time in which the patient reaches the criteria of Hospital discharge after the Gastric Bypass in y roux by Laparoscopic route with administration of Lidocaine perioperative intravenous route estimating the reduction in 12 hours in relation to the process of conventional anesthesia | — |
Countries
Brazil
Contacts
Public ContactRoclides de Lima
Universidade Federal de São Paulo
Outcome results
None listed