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Clinical Trial Summary

A randomized clinical trial to assess the effectiveness of same-day cervical preparation with oral, buccal or vaginal Misoprostol, given 2-4 hours prior first trimester curettage.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02480543
Study type Interventional
Source Wolfson Medical Center
Contact Hadas Ganer Herman, MD
Phone 972-077-2066960
Email hadassganer@yahoo.com
Status Recruiting
Phase Phase 4
Start date July 2015
Completion date July 2016

See also
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