Oral Misoprostol Versus Intravenous Oxytocin in Preventing Blood Loss After Non-Scheduled Cesarean Section

This study has been completed.
Sponsor:
Information provided by:
Basel Women’s University Hospital
ClinicalTrials.gov Identifier:
NCT00107874
First received: April 11, 2005
Last updated: June 23, 2005
Last verified: April 2005
No Study Results Posted on ClinicalTrials.gov for this Study
  Study Status: This study has been completed.
  Estimated Study Completion Date: February 2002
  Estimated Primary Completion Date: No date given