drugset / Trial / NCT02048098
Misoprostol for Second Trimester Termination of Pregnancy
RandomizedParallel-groupOpen-labelTreatment
Summary
The purpose of this study is to compare the efficacy of 400 µg vaginal misoprostol per 3 hours to 400 µg buccal misoprostol per 3 hours in second trimester termination of viable pregnancy
Timeline
- Start
- 2014-01
- Primary completion
- 2014-12
- Completion
- 2014-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Misoprostol | Other / unclassified | 400 ug | Intrathecal |
Indications
No indication recorded.