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Completed

NCT Number: NCT00451308

Induction of Labor With a Foley Balloon Catheter: Inflation With 30ml Compared to 60ml

The rate of labor induction is rising throughout the United States for a variety of reasons. Medical conditions that lead to increased risk of prolonging the pregnancy to both mother and fetus are not infrequent. In addition, elective deliveries are becoming more common. Foley balloon catheter placement is a common method used for labor induction in women with an unfavorable cervical assessment. There are several studies using various volumes of Foley balloon catheters for labor induction ranging from 30ml to 80ml, however, there are no studies replicating the findings of the largest study comparing 2 different volumes in the balloon. The investigators plan to compare instillation of 30ml of sterile saline versus 60ml in a Foley balloon catheter for women undergoing induction of labor with an unfavorable cervix. The investigators will observe the following outcomes: rate of delivery within 24 hours, cervical dilation after foley balloon catheter expulsion, insertion to balloon expulsion interval, induction to delivery time interval, peak oxytocin requirement, presence of infection or meconium, cesarean delivery rate, operative vaginal delivery rate, indication for operative vaginal or cesarean delivery, cervical laceration rate, placental abruption rate, 5-minute Apgar score, and umbilical cord arterial blood pH and base excess.

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Key information

Conditions

Sex eligibility

Female

Study type

Interventional

Phase

Phase 4

Primary location

University of California, San Francisco Department of Obstetrics, Gynecology and Reproductive Sciences

San Francisco, California, 94143, United States

About this study

All potential candidates will be approached for the study and undergo written consent if willing to participate. Each candidate will be randomized to 30ml or 60 ml Foley balloon catheter volume. A random number generator will be used and within a sealed envelope will be placed the assignment. Nulliparous and multiparous patients will be randomized separately. The patient will be positioned for a standard cervical exam - either for digital or speculum exam, depending on the individual patient preference and provider choice. For digital exam, a sterile Foley balloon catheter will be digitally placed in the endocervical canal, into the extraamniotic space (between the fetal head, external to the unruptured amniotic sac, above the internal os of the cervix). For speculum exam, the cervix is wiped three times with a Betadine cleansing solution, and a sterile Foley balloon catheter bulb will be placed under direct visualization into the endocervical canal, into the extraamniotic space. Once the balloon is in place the provider inserts 30ml of sterile saline. The provider then leaves the room. The patient's nurse opens the envelope and if the patient is allocated to the 60ml volume group, the nurse adds an additional 30ml of sterile saline. If the patient is in the 30ml group, the RN staff will simulate placement of additional saline into the foley balloon without actually placing any additional saline in order to also blind the patients to their assigned group. The MD/CNM providers will then return to the room, blinded to the inflation of the Foley balloon, and the balloon catheter will be placed under tension by taping the external end to the patient's inner thigh. Oxytocin will be started within 30 minutes of the Foley balloon catheter placement, using the standard intravenous oxytocin protocol. Additional manual traction on the Foley balloon catheter will be performed every 30 minutes until Foley balloon catheter expulsion. A sterile cervical exam will be performed after spontaneous Foley catheter expulsion to evaluate post-balloon cervical dilation. No further procedures or tests specific to this study will be required beyond this point; only data collection on the above study outcomes during the remaining course of the patient's labor will be recorded.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Reproductive aged women, pregnant, term gestation (>37 weeks), undergoing induction of labor, cervical exam acceptable as a candidate for Foley balloon catheter placement (Bishop score <5), cephalic fetal presentation.

Exclusion criteria

  • Regular contractions on admission, rupture of membranes, previous uterine scar, low-lying placenta (measured <3cm to internal os), Bishop score > 5, contraindication to attempt at vaginal birth, non-English/Spanish speaking, unable to give consent.

Treatment and study plan

Induction of labor with foley balloon - 60cc of saline

Procedure

60 cc of fluid

Induction of labor with foley balloon with 30cc

Procedure

30cc of saline in foley

Primary outcomes

  1. Rate of vaginal delivery within 24 hours

    Time frame: within 24 hours

Secondary outcomes

  1. Cervical dilation after Foley balloon catheter expulsion

    Time frame: within 24hours

  2. Time to catheter expulsion

    Time frame: hours

  3. Duration of the first stage of labor

    Time frame: hours

  4. Time interval from induction to active labor

    Time frame: hours

  5. Induction to delivery interval

    Time frame: hours

  6. Presence of abnormal vaginal bleeding

    Time frame: hours

  7. Peak oxytocin requirement during induction and labor augmentation

    Time frame: hours

  8. Epidural utilization, diagnosis of chorioamnionitis

    Time frame: hours

  9. Meconium stained amniotic fluid, placental abruption

    Time frame: hours

  10. Cesarean delivery rate, operative vaginal delivery rate

    Time frame: hours

  11. Indication for operative vaginal or cesarean delivery

    Time frame: hours

  12. Rate of cervical laceration

    Time frame: hours

  13. Birthweight

    Time frame: hours

  14. 5 minute Apgar score

    Time frame: hours

  15. Umbilical cord arterial blood pH analysis

    Time frame: hours

Sponsors and collaborators

Lead sponsor

University of California, San Francisco

Other

Registry information

Official study title

Induction of Labor With a Foley Catheter Balloon: A Randomized Trial Comparing Inflation With 30ml and 60ml

Important dates

Study start
2006
Primary completion
2009
Study completion
2009
First posted
Mar 23, 2007
Registry last updated
Aug 2, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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