effect of oral and vaginal evening primrose oil on cervical ripening and pregnancy outcomes and compare together

Not Applicable

Conditions: complications of labor and delivery.
Failed medical induction of labour

Registration Number: IRCT20171015036793N2

Lead Sponsor: vice chancellor for research of the Ahvaz Jundishapour University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Complete

Sex: Female

Target Recruitment: 90

Inclusion Criteria

cephalic presentation
alive fetus
with gestational age 40 weeks to42 weeks based on LMP or ultrasound in first trimester
Normal patterns of fetal heart rate
Without uterine contractions
cervical bishop score less than 4 intact membranous
Low-risk pregnancy
( have no known surgical and internal disease or pregnancy complication such as previa, abruption, preeclampsia , no known fetal problems)
Avoiding the enema
Avoiding the Intercourse

Exclusion Criteria

consumption of laxatives, the use of herbal medicines, chemical or traditional methods for induction of labor

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Ripening of cervix. Timepoint: during the labor. Method of measurement: bishop score table.

Secondary Outcome Measures

Name	Time	Method
Duration of first, second and third stage of labor. Timepoint: during the labor. Method of measurement: chronometer/examination/check list/observation.;Type of delivery. Timepoint: during the labor. Method of measurement: Separation into cesarean section and normal according to how the embryos leave.;Infant APGAR score. Timepoint: first and fifth minute after delivery. Method of measurement: apgar table.