Trials / Completed
CompletedNCT02981030
Acceptability and Feasibility of a Simplified Medical Abortion Service Delivery in Western Ukraine
Acceptability and Feasibility of a Simplified Medical Abortion Service Delivery in Western Ukraine: A Demonstration Study of 800 mcg Buccal Misoprostol Following 200 mg Mifepristone for Abortion up to 70 Days Gestation
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 102 (actual)
- Sponsor
- Gynuity Health Projects · Academic / Other
- Sex
- Female
- Age
- —
- Healthy volunteers
- Accepted
Summary
The study will examine how a simplified outpatient medical abortion procedure using mifepristone and misoprostol, with the option to take mifepristone at a place of woman's choosing, works in Ukraine. The investigators intend to demonstrate the efficacy of oral administration of 200 mg mifepristone and buccal administration of 800 mcg misoprostol with gestations through 70 days, as well as the acceptability of this method.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Mifepristone | Women seeking medical abortion will be offered the option to take mifepristone at home |
| DRUG | Misoprostol | Women seeking medical abortion will be offered the option to take misoprostol at home. Misoprostol will be administered buccally. |
Timeline
- Start date
- 2016-11-23
- Primary completion
- 2017-06-30
- Completion
- 2017-06-30
- First posted
- 2016-12-02
- Last updated
- 2018-06-18
Locations
2 sites across 1 country: Ukraine
Source: ClinicalTrials.gov record NCT02981030. Inclusion in this directory is not an endorsement.