About this trial
The goal of this randomized controlled trial is to examine the efficacy of combining castor oil ingestion with extra-amniotic single balloon catheter for cervical ripening on time from induction to delivery in multiparous women.
The main question it aims to answer are:
Does the addition of the use of castor oil to extra-amniotic single balloon reduce the time until birth? Does the addition of the castor oil affect other perinatal outcomes during childbirth? Are the side effects of the castor tolerated by the mothers? Participants will be randomly divided into 2 groups: the study group will drink a mixture of 60 ml of castor oil mixed with 140 ml of orange juice. Thirty minutes later, extra-amniotic single balloon catheter will be inserted above the internal cervical os and filled with 60 mL of normal saline.
In the control group, the catheter will be inserted into cervical canal without ingestion of castor oil.
Eligibility criteria
Qualifiers
Women above 18 years old
Sign an informed consent
Term pregnancy (>37 weeks)
Viable fetus
Disqualifiers
Previous cesarean delivery
Major fetal malformations
Contraindication to spontaneous vaginal delivery
Amniotic fluid index >25cm
Trial design
Treatments tested in this trial
- Induction of labor