Foley Catheter Versus Cervidil for Induction of Labor at Term

BACKGROUND:

Induction of labor is performed in 25% of all women who present for delivery at the Banner
Good Samaritan Medical Center (1). The commonality of labor induction is not only a local
issue. The national cesarean rate has risen to 31.1%, which represents a 50% increase since
1996 (2). Part of the reason for this increase in the cesarean delivery rate is the
pervasive use of labor induction. This risk can be mitigated with the use of cervical
ripening agents when a cervix is unfavorable for induction. Both pharmacological
(prostaglandin analogues) ripening agents and mechanical methods are utilized, but no single
method has been shown to offer a significant advantage over the other methods. Many centers,
including ours, have several different methods available, since each ripening method may
have one or more unique contraindications for their use during labor induction.

One emerging modality for cervical ripening and labor induction has been transcervical Foley
balloon catheter placement, which is thought to operate by mechanical dilation of the
cervix. The modality has become popular in part due to its efficacy, safety and low cost.
The most popular method of labor induction at Banner Good Samaritan Medical Center is a
controlled release prostaglandin application (Cervidil™). This modality is expensive and may
require more than one dose, thus increasing duration of labor induction and hospital costs.
A thorough literature search was performed on PubMed with the search terms "foley" "labor
induction" "prostaglandin E2 vaginal insert" from 1972 to 2009 and to date there have been
no randomized trials comparing the efficacy of these two modalities for labor induction.
Additionally, the clinical trials.gov site (www.clinicaltrials.gov) was searched and there
are no active or previously complete studies of Cervidil™ compared to transcervical Foley
balloon for labor induction. Therefore, we propose a randomized controlled clinical trial to
evaluate the comparative efficacies of these two modalities for cervical ripening and labor
induction in term and near term women.

METHODOLOGY:

All HIPAA and GCP regulations will be followed and IRB approval will be obtained.

This is a randomized controlled trial conducted at Banner Good Samaritan Medical Center
(BGSMC) and Banner Desert Medical Center (BDMC) beginning February 1, 2010 and continuing
until approximately 330 patients have been enrolled. Patients will be allocated by an online
randomization system either to transcervical Foley catheter or controlled release
prostaglandin (Cervidil™) in a 1:1 ratio. The Foley catheter used will be a 30cc/24 F. The
Foley bulb is placed in the cervix and a balloon is filled with water to apply pressure to
the cervix in order for the mechanical dilatation to occur. After the Foley catheter is
placed, the RN will check (by gently tugging) the placement of the catheter every 2 hours
until dislodged. Foley catheter will be removed either by spontaneous expulsion or after 12
hours if not expelled.

If the patient is randomized to the controlled release prostaglandin (Cervidil™) arm, a
controlled release prostaglandin (Cervidil™) will be placed in the posterior fornix of the
vagina to help ripen, or dilate and soften the cervix and removed after 12 hours. This
medication may be repeated for an additional 12 hours per the physicians orders and standard
of care procedures. The controlled release prostaglandin (Cervidil™) should be removed
sooner if tachysystole (defined as more than 5 uterine contractions in 10 minutes) is noted.

After expulsion of the Foley catheter or after 12 hours in either group, oxytocin will be
started according to the hospital's administration protocol. Otherwise, labor management
will be at the discretion of the attending physician. Prophylactic antibiotics will not be
administered unless indicated (GBS prophylaxis, chorioamnionitis develops during labor,
etc).

A master subject list will be generated. Data collection forms will assign unique patient
numbers starting with one and correlating with the master list. Data collection forms will
not contain patient names, but the master list will have a number correlated with the
patient ID. The data collection forms will collect demographic information including the
date of birth for statistical analysis. All lists will be kept confidential and stored under
locked conditions. The master list will be destroyed once the study is complete and the
final report has been written.

Variables:

Outcomes:

1. Primary: Time from start of induction to delivery

2. Secondary:

A. Proportion of patients delivered by 12 hours B. Proportion of patients delivered by
24 hours C. Proportion of patients delivered vaginally by 12 hours D. Proportion of
patients delivered vaginally by 24 hours E. Chorioamnionitis (defined as a temperature
of 38°C or higher and one of the following: maternal heart rate over 100, baseline
fetal heart rate over 160, uterine tenderness, and/or purulent or foul-smelling
cervical discharge) F. Endometritis (defined as a postpartum temperature of 38°C or
higher on 2 or more occasions and no other source of fever) G. Overall cesarean rate H.
Infection (Intrapartum, postpartum, cause of) I. Neonatal Information at delivery and
discharge status (birth weight, apgars, cord pH, anomalies, NICU admission, other
complications, neonatal death) J. Postpartum Information (Endometritis, Uterine
tenderness, Maternal HR > 100 BMP, Purulent cervical discharge, wond complications,
Ileus/Obstruction, Pneumonia, DVT/PTE (heparin treated) Intraperitoneal hematoma,
Intraperitoneal abscess, UTI, Pyelonephritis, Maternal ICU admission, Maternal death)
K. Date and time of Maternal and Neonatal discharge

3. Predictors:

A. Patient Demographics (date of birth, race, height, weight) B. Vital signs C. Maternal
Comorbidities (Chronic Hypertension, Gestational Hypertension, Diabetes, Obesity or BMI) D.
Induction Indications (Abnormal Antepartum Testing, Prior pregnancies, mode of deliveries,
Pre-eclampsia, > 41 weeks gestation, Group Beta Strep status E. Physical Exam (Sterile
vaginal exam, Membrane status) F. Study medication/device information (time of
administration, removal, success of placement) G. Other induction medications (if indicated)
H. Intrapartum antibiotics (if yes, reason for administration) I. Delivery data (date, time,
mode of delivery)

STATISTICAL ANALYSIS: Descriptive statistics will be used, with continuous variables
reported as means and standard deviations and categorical variables as percentages. T-tests
will be used to analyze continuous variables and the Chi square test for categorical
variables. Linear regression will be used to determine predictors of the primary outcome,
and logistic regression for categorical outcomes. A two-tailed p < 0.05 will be considered
significant.

SAMPLE SIZE CALCULATION: From review of the available literature evaluating these two
modalites for labor induction (in separate studies), we make the following assumptions for
our power calculation: 1. The mean time to delivery in the Cervidil group will be 24 hours.
2. The standard deviation for time to delivery in each group will be 15 hours. 3. A
clinically significant decrease in the time to delivery in the Foley group is 6 hours (to a
mean of 18 hours). With an alpha of 0.05 and 1-beta of 0.90, a sample size of 264 (132 in
each group) is needed. Allowing a 20% cesarean delivery rate, so that a separate analysis
can be performed for only those patients who delivered vaginally, the total number of women
needed to be enrolled is 330.

INTERIM DATA ANALYSIS:

Because of the novel nature of this comparative induction regimen, an interim analysis and a
futility analysis will be pursed when the first 100 of the study patients have been
enrolled. The futility analysis will help direct trial progress.

A Data Safety Monitoring Board (DSMB) will be in place at the start of the study. The DSMB
will comprise an independent obstetrician-gynecologist, a statistician and a bioethicist. It
will regularly review SAE's.

It will also conduct an interim analysis when 100 subjects have had deliveries. Using the
O'Brien-Fleming method, the p value for stopping the study due to superiority is 0.0051. At
the final analysis, the remaining alpha for determining superiority is 0.0477. For the
futility analysis, when 100 subjects have had a vaginal deliveries, a conditional power will
be calculated. If the conditional power is < 0.20, then the study will be halted due to
futility.

Inclusion Criteria:

1. Cervix < 3 cm dilated. If 2cm dilated, must be < 80% effaced.

2. Gestational age ≥ 36 weeks by best obstetric estimate, and clinical management
decision is delivery.

3. Singleton gestation

4. Cephalic presentation

Exclusion Criteria:

1. Regular uterine contractions (more frequent than every 5 minutes)

2. PROM

3. Prior transverse uterine incision or any obstetric contraindication to labor

4. Fever (defined as a temperature of 38°C or higher)

5. Lethal fetal anomalies (Labor induction is being performed, but there is no plan for
fetal heart rate monitoring or cesarean delivery for fetal indications.)

6. Fetal death

7. Placenta previa

8. Suspected placental abruption or undiagnosed bleeding characterized as more than
"spotting"

9. Non-reassuring fetal heart rate pattern

10. HIV