Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Efficacy & Safety Study Comparing Misoprostol Vaginal Insert (MVI) Versus Dinoprostone Vaginal Insert (DVI) for Reducing Time to Vaginal Delivery

ClinicalTrials.gov ID: NCT01127581

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.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 11:59 AM EDT

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

Study identification

NCT ID
NCT01127581
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ferring Pharmaceuticals
Industry
Enrollment
1,358 participants

Conditions and interventions

Interventions

  • MVI 200 Drug
  • Dinoprostone Vaginal Insert (DVI) Drug

Drug

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
Aug 31, 2010
Primary completion
Feb 29, 2012
Completion
Feb 29, 2012
Last update posted
Apr 30, 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 Apr 30, 2014 · Synced Jul 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01127581 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →