Patient Satisfaction of Cervical Ripening in an Outpatient Setting

Status unconfirmed · Not applicable

Conditions studied: Pregnancy

In brief

This study examines whether outpatient pre-induction cervical ripening improves patient satisfaction and is safe and effective.

Key facts

Study ID

NCT01605474

Run by

Cedars-Sinai Medical Center

People needed

800

Starts

2012-04-01

Last updated by the study team

2012-05-25

Who can join

Age: 18 and older, up to 60. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• term pregnancy
• singleton gestation
• cephalic presentation
• scheduled for an induction of labor (acceptable conditions include gestational diabetes, chronic hypertension)
• Exclusion criteria include the following:
• placenta previa and/or accreta
• low lying placenta
• undiagnosed vaginal bleeding
• preeclampsia
• fetal anomaly
• intrauterine growth restriction
• RH isoimmunization
• fetal demise
• rupture of membranes
• maternal heart disease
• known latex allergy
• active genital herpes infection
• previous uterine surgery
• limited access to a telephone
• excessive distance from the hospital, and/or
• unreliable transportation

Where it is running

• Cedars-Sinai Medical Center — Los Angeles, California, United States (enrolling)

Full record on ClinicalTrials.gov

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