Trials / Completed
CompletedNCT00386867
A Randomized Trial of Buccal Compared to Oral Misoprostol Following Mifepristone for Medical Abortion up to 63 Days LMP
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 1,200 (estimated)
- Sponsor
- Gynuity Health Projects · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
This open-label, randomized study will compare the efficacy, safety, and acceptability of mifepristone 200 mg followed in 24-36 hours either by buccal (i.e., in the cheeks) or oral misoprostol 800 mcg for termination of pregnancy in women up to 63 days L.M.P.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | 800 mcg misoprostol via oral or buccal administration |
Timeline
- Start date
- 2006-10-01
- Completion
- 2007-03-01
- First posted
- 2006-10-12
- Last updated
- 2007-06-05
Locations
8 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00386867. Inclusion in this directory is not an endorsement.