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
| Type | Name | Description |
|---|---|---|
| DRUG | misoprostol | 400mcg misoprostol, buccal administration, 1 time dosing 3-4 hours before abortion by D\&E |
| DEVICE | Dilapan-S, vitamin B-12 | One 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.