Now Available for Public Comment: Notice of Proposed Rulemaking (NPRM) for FDAAA 801 and NIH Draft Reporting Policy for NIH-Funded Trials

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

The recruitment status of this study is unknown because the information has not been verified recently.
Verified June 2008 by St. Luke's Hospital, Kansas City, Missouri.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
St. Luke's Hospital, Kansas City, Missouri
ClinicalTrials.gov Identifier:
NCT00695240
First received: June 9, 2008
Last updated: June 10, 2008
Last verified: June 2008
No Study Results Posted on ClinicalTrials.gov for this Study
  Study Status: This study is currently recruiting participants.
  Estimated Study Completion Date: July 2009
  Estimated Primary Completion Date: July 2009 (Final data collection date for primary outcome measure)