Status:
COMPLETED
Lidocaine and Outpatient Gynecologic Laparoscopy
Lead Sponsor:
Northwestern University
Conditions:
Pain
Eligibility:
FEMALE
18-64 years
Phase:
NA
Brief Summary
Although ambulatory gynecological laparoscopy is considered to be a minimally invasive surgical procedure, only 60% of patients undergoing this procedure are satisfied with postoperative pain control....
Detailed Description
70 subjects will be randomly allocated into 2 groups, using a computer generated table of random numbers. Group A (study group) will receive lidocaine. Group B (control group) will receive the same vo...
Eligibility Criteria
Inclusion
- Female patients undergoing outpatient laparoscopic gynecologic surgery
- American society of anesthesiologists class (ASA) Physical status (PS) I and II
- Age between 18 and 64 years
- Fluent in English
- Body mass index (BMI) less than 35
Exclusion
- History of allergy to local anesthetics
- History of chronic opioid use
- Pregnant patients
- Body Mass Index (BMI) greater than 35
- History of electrocardiogram (EKG) abnormalities
- Hepatic Impairment
- History of congestive heart failure
- Electrocardiogram (EKG) abnormalities
- History of heart block (subject with history of heart block)
- Current use of anti-arrhythmic medications
- Drop -Outs:
- Patient or surgeon request
- Conversion of the surgery from laparoscopic to open
Key Trial Info
Start Date :
November 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 1 2011
Estimated Enrollment :
70 Patients enrolled
Trial Details
Trial ID
NCT01250002
Start Date
November 1 2010
End Date
October 1 2011
Last Update
June 26 2014
Active Locations (1)
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1
Prentice Womens Hospital
Chicago, Illinois, United States, 60611