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)