Marcaine Use in Laparoscopic Gynecological Surgery

Stopped early · Not applicable

Conditions studied: Post-operative Pain

In brief

The purpose of this trial is to compare incisional pain in patients receiving pre-incisional versus post operative Marcaine injection.

Key facts

Study ID

NCT01861665

Run by

Weill Medical College of Cornell University

People needed

27

Starts

2010-06-01

Expected to finish

2017-01-01

Last updated by the study team

2018-10-12

Who can join

Age: 18 and older, up to 50. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• • 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

You may not qualify if…

• • 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

Where it is running

• Weill Cornell Medical College — New York, New York, United States

Full record on ClinicalTrials.gov

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