Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT02679092

Mifepristone Versus Osmotic Dilators in Conjunction With Misoprostol for Cervical Preparation Prior to D&E at 14-19 Weeks

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Stanford University · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

Dilation and evacuation (D\&E) is a common surgical procedure in the U.S. Adequate pre-operative preparation of the uterine cervix is an important part of preventing complications of the procedure. Traditionally, the uterine cervix is prepared for the procedure using water-attracting dilators, which are placed via a speculum exam and cause discomfort for many women. The objective of this study is to investigate the comparative effectiveness of mifepristone (an oral tablet) versus dilators for cervical preparation for D\&E.

Conditions

Interventions

TypeNameDescription
DRUGMisoprostol400 mcg buccal 60-90 minutes prior to procedure
DRUGMifepristone200 mg PO on the day prior to D\&E
DEVICEHygroscopic cervical dilatorsosmotic cervical dilators inserted through the internal os

Timeline

Start date
2016-04-01
Primary completion
2020-02-01
Completion
2020-12-01
First posted
2016-02-10
Last updated
2019-09-19

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02679092. Inclusion in this directory is not an endorsement.