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Clinical Trials/IRCT201507022248N17
IRCT201507022248N17Completed未知

The effect of oral Evening Primrose Oil on cervical ripening and pregnancy outcomes in nulliparous women

Vice Chancellor for research of the international branch of Iran University of Medical science0 sites80 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
80

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 years to 35 years (—)
Sex
Female

Inclusion Criteria

  • Inclusion criterias: cephalic presentation; alive fetus; with gestational age 40 weeks to (40 weeks + 6 days) 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; Maternal height more than 150 cm; non-addicted persons; normal adjusted BPP at the time of inclusion;An ultrasound of the placental grading;weight of fetus between 2500-4000 grams based on physical examination or ultrasonography; 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, Intercourse, laxatives, the use of herbal medicines, chemical or traditional methods for induction of labor; Lack of vaginal examination 24 hours before the begining till end of the study; Exclusion criterias: appears possible side effects of drugs such as headache, nausea, diarrhea and etc, those who consume them is less than two capsule per day, withdrew from the partnership at any stage of the study.

Exclusion Criteria

  • Not provided

Investigators

Sponsor
Vice Chancellor for research of the international branch of Iran University of Medical science

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