Trials / Withdrawn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- Withdrawn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
| Type | Name | Description |
|---|---|---|
| DRUG | Misoprostol | 400 mcg buccal 60-90 minutes prior to procedure |
| DRUG | Mifepristone | 200 mg PO on the day prior to D\&E |
| DEVICE | Hygroscopic cervical dilators | osmotic 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.