Post-Operative Pain Scores and Analgesic Requirements After Elective Inguinal Herniorrhaphy

This study has suspended participant recruitment.
(Need amendments in application process and require IBD number from FDA)
Sponsor:
Information provided by (Responsible Party):
University of Oklahoma
ClinicalTrials.gov Identifier:
NCT00735124
First received: August 13, 2008
Last updated: June 13, 2012
Last verified: June 2012
No Study Results Posted on ClinicalTrials.gov for this Study
  Study Status: This study has suspended participant recruitment.
  Estimated Study Completion Date: December 2012
  Primary Completion Date: December 2009 (Final data collection date for primary outcome measure)