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Compares treatment options for Labor Induction
Official title Cervical Ripening Balloon, 3 Hours vs 12 Hours Placement
ClinicalTrials.gov ID: NCT07689357
What this study is testing
- What it's testing
- The goal of this clinical trial is to learn if a shorter duration of cervical ripening balloon (CRB) placement can reduce the time to delivery in pregnant women undergoing induction of labor. The main questions it aims to answer are: Does placing the cervical ripening balloon for 3 hours or less result in a shorter interval from insertion to delivery compared to the standard 12-hour placement?
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 45, women only
You may be able to join if
- Nulliparous or multiparous pregnant women.
- Gestational age between 37 0/7 and 41 6/7 weeks of gestation.
- Maternal age between 18 and 45 years.
- Participant has provided signed informed consent.
You likely can't join if
- Presence of any contraindications for vaginal delivery.
- Multifetal gestation.
- Rupture of membranes prior to balloon insertion.
- Favorable cervix, defined as a Bishop score greater than 6.
- Cervical dilation greater than 2 cm.
- Previous cesarean delivery or any other prior major uterine surgery.
The study team makes the final eligibility decision.
Where it's taking place
- Haifa, Israel
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling female, 18 years to 45 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Haifa, Israel. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.