Abdominal and pelvic pain
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients aged 18 to 65 years; female; American Society of Anesthesiologists physical status - ASA I or II; undergoing total laparoscopic hysterectomy
Exclusion criteria
Exclusion criteria: Patients with severe comorbidity (American Society of Anesthesiologists physical status - ASA III or higher); cardiac arrhythmias; dilated cardiomyopathy; cardiac conduction disorder; electrolyte disorder; acid-base disorder; hypersensitivity to lidocaine; psychiatric, hepatic, respiratory or oncological diseases; patients who were receiving any type of analgesic in the week prior to surgery; patients who received blood products during the study period; and those whose health insurance does not cover the intervention procedures
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the analgesic efficiency of regional or spinal anesthesia techniques associated with general anesthesia by assessing the visual numerical pain scale, the time until the first request for morphine and the total morphine consumption in the postoperative period of laparoscopic hysterectomy. | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the incidence of postoperative nausea and vomiting through the consumption of antiemetics during hospitalization;Assess the presence of other adverse effects (dizziness, drowsiness, metallic taste, paresthesia, among others) through a questionnaire in the postoperative period | — |
Countries
Brazil
Contacts
Hospital São Domingos