A Trial of Cervidil for Outpatient Pre-induction of Cervical Ripening

Stopped early · Phase 3

Conditions studied: Induction of Labor Affected Fetus / Newborn

In brief

Induction of labor is a frequently planned obstetric procedure. Induction for women with an unfavorable cervix (bishop score \<6) increases the risk of cesarean section. This risk may be reduced by ripening or softening the cervix before the induction of labor. This protocol outlines a randomized trial of 200 women evaluating the placement and use of Cervidil to the post vaginal fornix to soften the cervix in preparation for induction. This trial is looking at inpatient vs outpatient pre-induction cervical ripening using Cervidil and the effects on (1) maternal and newborn outcomes including time of admission to delivery, (2) system healthcare cost, (3) cost to patient, and (4) patient satisfaction. The investigators hypothesize when compared to patients admitted to the hospital for cervical ripening: 1. From the time of admission, patients in the outpatient cervical ripening arm will progress to complete cervical dilation in less time. 2. The total overall cost of care for the encounter will be reduced for the group in the outpatient cervical ripening arm. 3. Patients in the outpatient cervical ripening arm will have more overall satisfaction.

Key facts

Study ID

NCT03806231

Run by

Intermountain Health Care, Inc.

People needed

8

Starts

2019-08-07

Expected to finish

2020-04-11

Last updated by the study team

2021-09-05

Who can join

Age: 18 and older, up to 41. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Accurate gestational age dating by Intermountain dating criteria placing the patient between 39 0/7 and 41 6/7 weeks gestational at time of cervical ripening
• Planning to undergo cervical ripening for induction of labor
• Participants must live <20 minutes away from the enrolling facility, or must stay < 20 minutes away.
• Pregnant women between the ages of 18 and 41 at the time of enrollment.
• Fetus in vertex position

You may not qualify if…

• Gestational age < 39 weeks or > 41 weeks and 6 days
• Hypertension (chronic, transitional, gestational, preeclampsia)
• Multiple gestation
• Intrauterine Growth Restriction
• Anticoagulant therapy or at high risk for thromboembolism
• Cardiac disease other than class I per American Heart Association (AHA)
• Prior incision in the contractile portion of the uterus
• Placenta previa
• Oligohydramnios per American College of Obstetricians and Gynecologists (ACOG) criteria: AFI < 5 or deepest vertical pocket <= 2
• Polyhydramnios per ACOG criteria: Amniotic Fluid Index (AFI) >= 24
• Cervical dilation >= 3cm
• Known fetal anomaly that would require advanced neonatal care
• Pitocin-induction of labor is otherwise contraindicated
• Patient is receiving other uterotonics (e.g. oxytocin, Cytotec, etc.)
• Fetal distress
• Unexplained vaginal bleeding during the pregnancy
• Sensitivity to prostaglandin
• Evidence of or suspicion of marked cephalo-pelvic disproportion (per the Cervidil package insert revision 02/2016, Ferring Pharmaceuticals Inc. Parsippany, NJ)

Where it is running

• Dixie Regional Medical Center — St. George, Utah, United States

Full record on ClinicalTrials.gov

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