drugset / Trial / NCT03346629
Outpatient Service for Mid-trimester Termination of Pregnancy
Phase 4
Completed
230 enrolled
Gynuity Health Projects
CREHPA · collabKIST Medical College · collabKathmandu Medical College and Teaching Hospital · collabKathmandu Model Hospital · collab
NaSingle-groupOpen-labelTreatment
Summary
This study seeks to evaluate the safety, acceptability and feasibility of an outpatient "day procedure" for medical abortion at 13-18 weeks gestation. The study regimen will consist of a single dose of 200 mg mifepristone to be taken orally either at home or at the hospital, followed approximately 24 - 48 hours later with administration of 400 mcg misoprostol. Repeat doses of 400 mcg (two tablets) of misoprostol will be administered buccally every three hours until the abortion is achieved.
Timeline
- Start
- 2017-12-01
- Primary completion
- 2018-12-31
- Completion
- 2018-12-31
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Mifepristone | Small molecule | 200 mg | Oral |
| Subject | Misoprostol | Other / unclassified | 400 ug | Other |
Indications
No indication recorded.