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Misoprostol Versus Dilapan-S for Cervical Preparation

Cervical Ripening Clinical Trial

Official title:
Cervical Preparation Before Same-day Second Trimester Abortion With Buccal Misoprostol Versus Dilapan-S: A Randomized Placebo Controlled Trial

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

Clinical Trial Details
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
View Details
See also
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Completed NCT01170819 - Double Balloon Catheter Versus Dinoprostone Vaginal Insert for Cervical Ripening. Phase 4
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