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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:
ClinicalTrials.gov Identifier:
NCT00373789
First Posted: September 8, 2006
Last Update Posted: January 11, 2011
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
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: