PACTR201702002017237Completed未知
Postpartum vaginal blood loss following two different methods of cervical ripening
Okon A Okon0 sites82 target enrollmentStarted: February 3, 2017Last updated:
Trial Snapshot
- Phase
- 未知
- Status
- Completed
- Sponsor
- Enrollment
- 82
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 Year(s) to 48 Year(s) (—)
- Sex
- Female
Inclusion Criteria
- •37 completed weeks up to 41 completed weeks plus 3 days
- •Bishop score of <5
- •a live singleton fetus with cephalic presentation at term
- •intact membranes with no evidence of labor
- •no contraindications to a vaginal delivery
- •up to the third parity
Exclusion Criteria
- •history of uterine scar
- •breech presentation
- •fetal anomalies
- •antepartum hemorrhage
- •polyhydramnios
- •presence of uterine fibroids in pregnancy
- •known allergy to prostaglandin preparations
- •women with anemia (defined as hemoglobin level less than 10.5g/dl or a hematocrit of less than 31%)
- •bleeding disorders
- •pelvic abnormalities/deformities
Investigators
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