cervical ripening and termination of term pregnancy
Not Applicable
- Conditions
- vaginal delivery.Spontaneous vertex delivery
- Registration Number
- IRCT2016050527643N2
- Lead Sponsor
- Vice Chancellor for Research of Sabzevar University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 96
Inclusion Criteria
term pregnancy ; bishop score less than 6 ; cephalic presentation ; singleton pregnancy
Exclusion criteria:use of another way for cervical ripenig ; contraindication of labor inducton or NVD ; mother's comorbidity ; rupture of fetus membrane ; severe preeclampsia ; vaginal bleeding ; Placenta previa ; having a spontaneous contraction
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Cervical ripening. Timepoint: On admissiom and 12 hours later and before insertion of each dose. Method of measurement: Vaginal exam based on Bishop score.
- Secondary Outcome Measures
Name Time Method Maternal complications (Over stimulation of the uterus, headaches, tachycardia, hypotension, nausea, vomiting, and dizziness). Timepoint: During at the intervention. Method of measurement: Observation and Examination.;Method of delivery. Timepoint: During at the intervention. Method of measurement: Observation and Examination.;Duration of the first stage of labor. Timepoint: Active stage of labor. Method of measurement: Hour.;Neonatal outcomes (Apgar score at first and fifth minutes, birth weight, hospitalization of neonate in the Neonatal Intensive Care Unit). Timepoint: During at the intervention. Method of measurement: Observation and Examination.;Necessity of induction. Timepoint: During at the intervention. Method of measurement: Observation and Examination.