Comparison of effects of vaginal misoprostol tablet with vaginal evening primrose capsule on ripening of the cervix in nulliparous women

Shahid Beheshti University of Medical Sciences0 个研究点目标入组 90 人开始时间: 待定最近更新: 2018年3月26日

适应症

试验速览

暂无简介。

•18-35 years old First pregnancy Singleton pregnancy Presentation of fetal cephalic Live fatal Gestational age 40 weeks based on the first day of the last menstruation and first trimester Medical ultrasound Natural pattern of fetal heartbeat No uterine contractions Bishop score less than 4 Healthy amniotic bag Mother's height is more than 150 cm BMI less than 30 Not having drug abuse Natural biophysical profiling test at the time of starting the study Having an ultrasound for pair grading (zero and one Grade) Estimated fetal weighing 2500-4000 gr based on manual examination of the abdomen or ultrasound Low risk pregnancy (Not suffering from known internal and surgical diseases and complications of pregnancy such as previa, abruption, preeclampsia, and the absence of known fetal problems) No vaginal examination a 24 hours before starting the study Avoid doing enema, sexual intercourse, laxative, herbal medicines including castor oil and homeopathic remedies, chemotherapy, breast stimulation and traditional methods of initiating Birth pain 24 hours before the start of study until the end

•Any problems that require emergency action, such as not moving the fetus, mother's bleeding Get any herbal medicine during the study period Intercourse during the study possible side effects of the drug Cancellation of participation in the study at each stage

发起方