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Clinical Trial Summary

The main objective of the study is to determine if there is a difference in the number of women with a complete miscarriage after 10 days between expectant management versus treatment with 800 micrograms of misoprostol intravaginally in women with an an incomplete miscarriage before 14 weeks and a gestational sac retained in the uterus.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01033903
Study type Interventional
Source Region Skane
Contact
Status Completed
Phase N/A
Start date October 1, 2008
Completion date March 1, 2018

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