Oral Misoprostol Versus Intravenous Oxytocin in Preventing Blood Loss After Non-Scheduled Cesarean Section
This study has been completed.
Sponsor:
Basel Women’s University Hospital
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
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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 |