Clinical Trials Directory

Trials / Completed

CompletedNCT00835731

Misoprostol Versus Dilapan-S for Cervical Preparation

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
125 (actual)
Sponsor
Planned Parenthood League of Massachusetts · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGmisoprostol400mcg misoprostol, buccal administration, 1 time dosing 3-4 hours before abortion by D\&E
DEVICEDilapan-S, vitamin B-12One Dilapan-S rod placed in the cervix 3-4 hours before abortion by D\&E. Control: 1000mcg vitamin B-12, buccal administration 3-4 hours before abortion by D\&E

Timeline

Start date
2009-01-01
Primary completion
2011-12-01
Completion
2011-12-01
First posted
2009-02-04
Last updated
2017-10-23
Results posted
2014-01-07

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00835731. Inclusion in this directory is not an endorsement.