drugset / Trial / NCT00374621
Trial of Cervical Ripening and Labor Induction Using Misoprostol With or Without Intravaginal Isosorbide Mononitrate
RandomizedSingle-groupOpen-labelTreatment
Summary
The purpose of this study is to determine the efficacy and safety of the addition of intravaginal isosorbide mononitrate to an established protocol of oral misoprostol for cervical ripening and labor induction.
Timeline
- Start
- 2006-09
- Primary completion
- 2007-12
- Completion
- 2010-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Isosorbide Mononitrate | Other / unclassified | 40 mg | Other |
| Comparator | Misoprostol | Other / unclassified | 100 ug | Oral |