Misoprostol Versus Dilapan-S for Cervical Preparation



Status:Completed
Conditions:Women's Studies
Therapuetic Areas:Reproductive
Healthy:No
Age Range:18 - Any
Updated:10/25/2017
Start Date:January 2009
End Date:December 2011

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

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.


Inclusion Criteria:

- medically eligible for dilation and evacuation at Planned Parenthood League of
Massachusetts

- gestational age 12 weeks 0 days to 15 weeks 0 days as evaluated by ultrasound

- proficient in English or Spanish

- agreeing to study procedures, including randomization and surveys regarding
demographics, medical and gynecological history, and assessments of pain and
satisfaction

Exclusion Criteria:

- less than 18 years old

- cervical or uterine anomaly that the research physician deems may affect the
difficulty of dilation or the abortion procedure

- inflammatory bowel disease

- contraindication to misoprostol use

- known intolerance or allergy to misoprostol or Dilapan-S

- inability to give informed consent
We found this trial at
1
site
Boston, Massachusetts 02215
?
mi
from
Boston, MA
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