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Clinical Trial Summary

The purpose of this study is to compare the dilatory effect of 400 mcg of buccally administered misoprostol to one Dilapan-S rod placed 3-4 hours before abortion by dilation and evacuation in women who are 12 weeks 0 days to 15 weeks 0 days gestation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00835731
Study type Interventional
Source Planned Parenthood League of Massachusetts
Contact
Status Completed
Phase N/A
Start date January 2009
Completion date December 2011

See also
  Status Clinical Trial Phase
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Completed NCT01127581 - Efficacy & Safety Study Comparing Misoprostol Vaginal Insert (MVI) Versus Dinoprostone Vaginal Insert (DVI) for Reducing Time to Vaginal Delivery Phase 3
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Completed NCT01170819 - Double Balloon Catheter Versus Dinoprostone Vaginal Insert for Cervical Ripening. Phase 4
Completed NCT00442663 - Trial of Foley Catheter With and Without Extra-Amniotic Saline Infusion for Labor Induction N/A