Postoperative pain after laparoscpy. Acute pain
Conditions
Interventions
Intervention 1: With induction of anesthesia, lidocaine group will receive lidocaine infusion in the rate of 2mg/kg/h. Intervention 2: Control group will only receive normal saline in the same volume
Prevention
Treatment - Drugs
With induction of anesthesia, lidocaine group will receive lidocaine infusion in the rate of 2mg/kg/h
Control group will only receive normal saline in the same volume and infusion rate.
Sponsors
Vice Chancellor for research of Tabriz university of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria:Women candidate for Gynecologic Laparoscopic surgery; patients with ASA physical status I and II Exclusion criteria: Patient's with ASA class III or above; women with cardiovascular; respiratory diseases; hepatic or renal dysfunction; endocrine disorders; hypertension; psychologic disorder; convulsion; algeria to lidocaine; patients who received opioid or non opioid analgesic preoperatively
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: 2, 4, 6, 12, 24 hours postoperative. Method of measurement: Visual Analog Scale (VAS). | — |
Secondary
| Measure | Time frame |
|---|---|
| Rescue analgesic consumption after surgery. Timepoint: 24 hours postoperative. Method of measurement: Total dose mg.;The first analgesia administration. Timepoint: The time to the first analgesia administration. Method of measurement: Hours. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. farnaz Moslemi
Tabriz University of Medical Sciences
Outcome results
None listed