Intravenous Lidocaine in Bariatric Surgery. (XYLOBAR)
Morbid Obesity, Bariatric Surgery Candidate
About this trial
This is an interventional treatment trial for Morbid Obesity focused on measuring bariatric surgery, rehabilitation, lidocaine
Eligibility Criteria
Inclusion Criteria:
- scheduled bariatric surgery
Exclusion Criteria:
- any contra-indication for lidocaine administration
- pregnancy
- ASA class 4
- psychiatric disorder
- chronic opioid consumption
Sites / Locations
- University Hospital of Caen
Arms of the Study
Arm 1
Arm 2
Placebo Comparator
Experimental
Control
Lidocaine
intravenous isotonic saline administration : bolus of 0.075 ml/kg (adjusted body weight) at induction of anesthesia followed by a continuous infusion (0.1 ml/kg/h, adjusted body weight) until the end of surgery decrease to 0.05 ml/kg (adjusted body weight) during 60 min in post anesthesia care unit. Speed of infusion were calculated to be equivalent to that of lidocaine speed of injection.
Intravenous Lidocaine (20mg/ml) : bolus of 1.5 mg/kg (adjusted body weight) at induction of anesthesia followed by a continuous infusion (2.0 mg/kg/h, adjusted body weight) until the end of surgery decrease to 1.0 mg/kg (adjusted body weight) during 60 min in post anesthesia care unit.