Trials / Completed
CompletedNCT00393731
A Randomized, Control Trial for Preinduction Cervical Ripening
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 540 (estimated)
- Sponsor
- The University of Texas Health Science Center, Houston · Academic / Other
- Sex
- Female
- Age
- —
- Healthy volunteers
- —
Summary
The goal of this study is to compare the vaginal delivery rates in women undergoing induction of labor with an unripe cervix between oxytocin induction alone and preinduction cervical ripening with prostaglandin El (misoprostol). Secondary goals are to measure and compare the time intervals to delivery between the two methods.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Misoprostol | |
| DRUG | oxytocin |
Timeline
- Start date
- 2004-01-01
- Primary completion
- 2007-08-01
- Completion
- 2007-08-01
- First posted
- 2006-10-30
- Last updated
- 2008-01-16
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00393731. Inclusion in this directory is not an endorsement.