A Randomized Controlled Trial of Sequential Versus Simultaneous Use of Foley Balloon and oxytocin for Induction of Labor in Nulliparous pregnant wome
Not Applicable
Recruiting
- Conditions
- Pregnancy and ChildbirthMaternal health - Induction of labor
- Registration Number
- PACTR201709002509200
- Lead Sponsor
- Saint Paul's Hospital Millennium Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 140
Inclusion Criteria
Nulliparous women 28 weeks¿ gestational age; with a live, non-anomalous singleton fetus in vertex presentation; with an initial cervical dilation <3 cm; who were admitted for induction of labor for indications determined by their primary provider; and in whom cervical ripening with Foley balloon was planned are eligible for enrollment.
Exclusion Criteria
Patients with prior uterine surgery, unexplained vaginal bleeding, any history of latex allergy or any contraindication to vaginal delivery will be excluded.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method