Trials / Completed
CompletedNCT02314754
Outpatient Medical Abortion With Mifepristone and Misoprostol Through 77 Days of Gestation
Outpatient Medical Abortion With Mifepristone and Misoprostol Through 77 Days of Gestation: A Non-inferiority Trial
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 719 (actual)
- Sponsor
- Gynuity Health Projects · Academic / Other
- Sex
- Female
- Age
- 11 Years – 55 Years
- Healthy volunteers
- Accepted
Summary
To demonstrate non-inferiority of the efficacy of 200 mg mifepristone followed in 24 to 48 hours by 800 µg buccal misoprostol in outpatient medical abortion services among women 71-77 days' compared to women 64-70 days' LMP.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Mifepristone followed by misoprostol 24-48 hours later | 200mg oral mifepristone and 800mcg buccal misoprostol 24-48 hours after mifepristone |
Timeline
- Start date
- 2014-12-01
- Primary completion
- 2016-04-01
- Completion
- 2016-04-01
- First posted
- 2014-12-11
- Last updated
- 2016-07-14
Locations
8 sites across 5 countries: United States, Azerbaijan, Georgia, Mexico, Vietnam
Source: ClinicalTrials.gov record NCT02314754. Inclusion in this directory is not an endorsement.