Surgical Pain Control With Ropivacaine by Atomized Delivery
Completed · Phase 4 · Has a placebo group
Conditions studied: Pain
In brief
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 used to block pain in the body. There are studies showing that Ropivacaine decreases the pain of surgery with minimally invasive (laparoscopic) appendix and gallbladder removal but has not been tried in robotic pelvic surgery.
Key facts
- Study ID
- NCT01480089
- Run by
- Loyola University
- People needed
- 56
- Starts
- 2011-11-01
- Expected to finish
- 2013-02-01
- Last updated by the study team
- 2016-07-27
Who can join
Age: 18 and older, up to 75. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- 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
You may not qualify if…
- Patients with an allergy to local anesthetics
- Patients with severe underlying cardiovascular, renal or hepatic disease
- Pregnant patients
Where it is running
- Loyola University Medical Center — Maywood, Illinois, United States
Full record on ClinicalTrials.gov
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