Status:
TERMINATED
Marcaine Use in Laparoscopic Gynecological Surgery
Lead Sponsor:
Weill Medical College of Cornell University
Conditions:
Post-operative Pain
Eligibility:
FEMALE
18-50 years
Phase:
NA
Brief Summary
The purpose of this trial is to compare incisional pain in patients receiving pre-incisional versus post operative Marcaine injection.
Detailed Description
Post-operative pain control is a key component of a patient's experience with surgery. In laparoscopic surgery, small (5 to 12mm) incisions are made, usually at the umbilicus and/on at either side of ...
Eligibility Criteria
Inclusion
- • Ages 18-50
- BMI 20-35
- Gynecologic ambulatory cases only
- Total of 3 incisions, with left and right incisions both being 5mm-10mm in size
- Not taking pain medications prior to surgery
- Length of surgery up to 3 hours
- PACU stay up to 6 hours
- Willing and able to sign informed consent
Exclusion
- • Age or BMI out of range
- Surgery longer than 3 hours or PACU stay longer than 6 hours
- patients with chronic pelvic pain
- Oncologic cases
- Pregnant patients
Key Trial Info
Start Date :
June 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2017
Estimated Enrollment :
27 Patients enrolled
Trial Details
Trial ID
NCT01861665
Start Date
June 1 2010
End Date
January 1 2017
Last Update
October 12 2018
Active Locations (1)
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1
Weill Cornell Medical College
New York, New York, United States, 10021