drugset / Trial / NCT00482209
Study of 400mcg Versus 800mcg Buccal Misoprostol Following Mifepristone 200mg for Abortion up to 63 Days Gestation
RandomizedParallel-groupDouble-blindTreatment
Summary
This double-blind, randomized study will compare the efficacy and acceptability of mifepristone 200mg followed in 36-48 hours by 400mcg or 800mcg of buccal misoprostol (i.e., in the cheeks) for termination of pregnancy in women up to 63 days LMP.
Timeline
- Start
- 2007-05
- Primary completion
- 2009-10
- Completion
- 2009-10
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Mifepristone | Small molecule | 200 mg | — |
| Comparator | Misoprostol | Other / unclassified | 400 ug | Other |
| Comparator | Misoprostol | Other / unclassified | 800 ug | Other |
Indications
No indication recorded.