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Clinical Trial Summary

This study compares oxytocin infusion to spontaneous follow-up for third-stage of labor at induced mid-trimester abortions. Patients will be randomized to oxytocin infusion or observation with no pharmacologic intervention. Primary outcome of the study is complete abortion rate within two hours of fetal delivery.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02485444
Study type Interventional
Source Ataturk University
Contact
Status Completed
Phase Phase 4
Start date June 8, 2015
Completion date June 10, 2016

See also
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