Status:
COMPLETED
Surgical Pain Control With Ropivacaine by Atomized Delivery
Lead Sponsor:
Loyola University
Conditions:
Pain
Eligibility:
FEMALE
18-75 years
Phase:
PHASE4
Brief Summary
The purpose of this trial is to determine the effect of spraying a local anesthetic called Ropivacaine (numbing medicine) into the abdominal cavity prior to surgery. Ropivacaine is a local anesthetic ...
Detailed Description
Practice guidelines from the American Society of Anesthesiologists peri-operative techniques for pain management have remained essentially unchanged over the last 10 years (3). Current acute pain-mana...
Eligibility Criteria
Inclusion
- Consent to undergo robotic assisted gynecologic or urologic surgery
- Between the ages of 18 and 75
- Able to consent, fill out study documents, and complete all study procedures and follow-up visits
Exclusion
- Patients with an allergy to local anesthetics
- Patients with severe underlying cardiovascular, renal or hepatic disease
- Pregnant patients
Key Trial Info
Start Date :
November 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 1 2013
Estimated Enrollment :
56 Patients enrolled
Trial Details
Trial ID
NCT01480089
Start Date
November 1 2011
End Date
February 1 2013
Last Update
July 27 2016
Active Locations (1)
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1
Loyola University Medical Center
Maywood, Illinois, United States, 60153