Refractory Urge Incontinence and Botox Injections

This study has been terminated.
(higher than anticipated rate of increased post-void residual in subjects who received botulinum toxin A injection)
Sponsor:
Information provided by:
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
ClinicalTrials.gov Identifier:
NCT00373789
First received: September 6, 2006
Last updated: January 9, 2011
Last verified: October 2010
No Study Results Posted on ClinicalTrials.gov for this Study
  Study Status: This study has been terminated.
  Study Completion Date: December 2007
  Primary Completion Date: December 2007 (Final data collection date for primary outcome measure)
Publications: