Trial of Cervical Ripening and Labor Induction Using Misoprostol With or Without Intravaginal Isosorbide Mononitrate
| Status: | Completed |
|---|---|
| Conditions: | Women's Studies |
| Therapuetic Areas: | Reproductive |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 4/26/2017 |
| Start Date: | September 2006 |
| End Date: | January 2010 |
Randomized Clinical Trial of Cervical Ripening and Labor Induction Using Stepwise Oral Misoprostol With or Without Intravaginal Isosorbide Mononitrate
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.
intravaginal isosorbide mononitrate to an established protocol of oral misoprostol for
cervical ripening and labor induction.
Inclusion Criteria::
- Pregnant women
- 18 years of age or greater
- Singleton pregnancy between 32-42 weeks gestation requiring labor induction
- Membranes must be intact
Exclusion Criteria:
- Ruptured membranes
- Gestational age less than 32 weeks
- Non-reassuring fetal heart rate tracing
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Stanford University School of Medicine Vast in both its physical scale and its impact on...
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