Status:
UNKNOWN
Post-Operative Pain Control Using Direct Continuous Bupivacaine Infusion After Pelvic Organ Prolapse Repair
Lead Sponsor:
St. Luke's Hospital, Kansas City, Missouri
Conditions:
Post-Operative Pain
Pelvic Organ Prolapse
Eligibility:
FEMALE
18+ years
Phase:
PHASE2
PHASE3
Brief Summary
This prospective randomized controlled study will determine the efficacy of continuous local anesthesia at decreasing pain scores compared to patient controlled analgesia for pelvic organ prolapse pro...
Detailed Description
Direct post-operative analgesia can be administered via a direct continuous analgesia pumps providing local anesthetic into a dissected area. To date, no studies have been conducted to evaluate pain c...
Eligibility Criteria
Inclusion
- Female patients greater than 18 years of age
- Undergoing posterior colporrhaphy at Saint Lukes Hospital, Kansas City, MO.
Exclusion
- Patients with chronic pain conditions requiring daily narcotics were excluded
Key Trial Info
Start Date :
April 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
July 1 2009
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT00695240
Start Date
April 1 2007
End Date
July 1 2009
Last Update
June 11 2008
Active Locations (1)
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1
St. Luke's Hospital
Kansas City, Missouri, United States, 64108