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

Clinical trial NCT00695240 · UNKNOWN

Trial details

NCT number: NCT00695240
Sponsor: St. Luke's Hospital, Kansas City, Missouri
Status: UNKNOWN
Phase: Phase 2, Phase 3
Study type: INTERVENTIONAL

Post-Operative Pain Pelvic Organ Prolapse

Start date: 2007-04-01
Primary completion: 2009-07-01
Enrollment: 80

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