Evaluation of the effect of perioperative intravenous infusion of lidocaine in postoperative pain management in women under gynecologic laparoscopy

Not Applicable

• Conditions: Postoperative pain after laparoscpy.; Acute pain; R50,R51,R5

• Registration Number: IRCT2014040511700N5
• Lead Sponsor: Vice Chancellor for research of Tabriz university of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 60

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

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: 2, 4, 6, 12, 24 hours postoperative. Method of measurement: Visual Analog Scale (VAS).

Secondary Outcome Measures

Name	Time	Method
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.