Post-Operative Pain Control Using Direct Continuous Bupivacaine Infusion After Pelvic Organ Prolapse Repair

Status unconfirmed · Phase 2/Phase 3

Conditions studied: Post-Operative Pain, Pelvic Organ Prolapse

In brief

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 procedures including posterior colporrhaphy and sacrospinous ligament fixation.

Key facts

Study ID

NCT00695240

Run by

St. Luke's Hospital, Kansas City, Missouri

People needed

80

Starts

2007-04-01

Expected to finish

2009-07-01

Last updated by the study team

2008-06-11

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Female patients greater than 18 years of age
• Undergoing posterior colporrhaphy at Saint Lukes Hospital, Kansas City, MO.

You may not qualify if…

• Patients with chronic pain conditions requiring daily narcotics were excluded

Where it is running

• St. Luke's Hospital — Kansas City, Missouri, United States (enrolling)

Full record on ClinicalTrials.gov

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