ClinicalTrials.gov record
Completed Not applicable Interventional Accepts healthy volunteers Results available

Foley Catheter Versus Cervidil for Induction of Labor at Term

ClinicalTrials.gov ID: NCT01402050

Public ClinicalTrials.gov record NCT01402050. 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 May 17, 2026, 6:21 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

A Randomized Controlled Trial of Transcervical Foley Balloon Compared to Controlled Release Prostaglandin (Cervidil) for Labor Induction and Cervical Ripening in Term and Near Term Women

Study identification

NCT ID
NCT01402050
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Pediatrix
Other
Enrollment
376 participants

Conditions and interventions

Interventions

  • CERVIDIL (Dinoprostone) Drug
  • FOLEY BALLOON Device

Drug · Device

Eligibility (public fields only)

Age range
18 Years to 45 Years
Sex
Female
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 31, 2010
Primary completion
Oct 31, 2014
Completion
Jan 31, 2015
Last update posted
Mar 1, 2020

2010 – 2015

United States locations

U.S. sites
2
U.S. states
1
U.S. cities
2
Facility City State ZIP Site status
Banner Desert Medical Center Mesa Arizona 85210
Banner Good Samaritan Medical Center Phoenix Arizona 85006

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 NCT01402050, 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 Mar 1, 2020 · Synced May 17, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01402050 live on ClinicalTrials.gov.

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