Efficacy & Safety Study Comparing Misoprostol Vaginal Insert (MVI) Versus Dinoprostone Vaginal Insert (DVI) for Reducing Time to Vaginal Delivery
Public ClinicalTrials.gov record NCT01127581. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
Phase III, Double-blind, Randomized, Multicenter Study of Exogenous Prostaglandin Comparing the Efficacy & Safety of the MVI 200 mcg Versus the Dinoprostone Vaginal Insert (DVI) for Reducing Time to Vaginal Delivery in Pregnant Women at Term
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
The purpose of this study is to determine whether the Misoprostol Vaginal Insert (MVI) 200 microgram (mcg) can decrease the time to vaginal delivery compared to the Dinoprostone Vaginal Insert (DVI) 10 milligram (mg) in pregnant women requiring cervical ripening and induction of labor.
Study identification
- NCT ID
- NCT01127581
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 3
- Enrollment
- 1,358 participants
Conditions and interventions
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- Female
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Sep 2010 (Type not available)
- Primary completion
- Mar 2012 (Actual)
- Completion
- Mar 2012 (Actual)
- Last update posted
- May 1, 2014
2010 – 2012
United States locations
- U.S. sites
- 34
- U.S. states
- 20
- U.S. cities
- 31
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Maricopa Medical Center - District Medical Group | Phoenix | Arizona | — | — |
| Precision Trials | Phoenix | Arizona | — | — |
| Phoenix Perinatal Associates (Scottsdale Healthcare Shea) | Scottsdale | Arizona | — | — |
| Watching Over Mothers and Babies Foundation | Tucson | Arizona | — | — |
| Miller's Childrens Hospital | Long Beach | California | — | — |
| UCI Medical Center | Orange | California | — | — |
| The Women's Clinic of Northern Colorado | Fort Collins | Colorado | — | — |
| Christiana Care Health System (DE Center for MFM) | Newark | Delaware | — | — |
| University of FL College of Medicine | Jacksonville | Florida | — | — |
| Altus Research | Lake Worth | Florida | — | — |
| University of South Florida | Tampa | Florida | — | — |
| Indiana University School of Medicine | Indianapolis | Indiana | — | — |
| University of Kansas School of Medicine | Kansas City | Kansas | — | — |
| University of Michigan Hospital | Ann Arbor | Michigan | — | — |
| Spectrum Health | Grand Rapids | Michigan | — | — |
| St. Louis University | St Louis | Missouri | — | — |
| St. Peters University Hospital | New Brunswick | New Jersey | — | — |
| University of New Mexico/New Mexico Health Science Center | Albuquerque | New Mexico | — | — |
| Duke University Medical Center | Durham | North Carolina | — | — |
| East Carolina University, Brody School of Medicine | Greenville | North Carolina | — | — |
| Lyndhurst Gynecologic Associates | Winston-Salem | North Carolina | — | — |
| University of Cincinnati | Cincinnati | Ohio | — | — |
| Clinical Trials of America | Eugene | Oregon | — | — |
| Drexel University College of Medicine | Philadelphia | Pennsylvania | — | — |
| Temple University School of Medicine | Philadelphia | Pennsylvania | — | — |
| Thomas Jefferson University | Philadelphia | Pennsylvania | — | — |
| Medical University of South Carolina | Charleston | South Carolina | — | — |
| University Medical Group/Greenville Hospital System | Greenville | South Carolina | — | — |
| UT College of Medicine Chattanooga, Erlanger Health System | Chattanooga | Tennessee | — | — |
| High Risk Obstetrical Consultants, PLLC | Knoxville | Tennessee | — | — |
| Research Memphis Associates | Memphis | Tennessee | — | — |
| University of Texas Health Sciences Center at Houston | Houston | Texas | — | — |
| Salt Lake Women's Center, PC | Sandy City | Utah | — | — |
| Marshfield Clinic Research Foundation | Marshfield | Wisconsin | — | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT01127581, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted May 1, 2014 · Synced Oct 21, 2026
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Open the official record
The complete public registry record, listed eligibility criteria, and available contact information for NCT01127581 live on ClinicalTrials.gov.