Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Boston, Massachusetts 02215


Purpose:

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.


Criteria:

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


NCT ID:

NCT00835731


Primary Contact:

Principal Investigator
Prinicpal Investigator
Planned Parenthood League of Massachusetts


Backup Contact:

N/A


Location Contact:

Boston, Massachusetts 02215
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.