跳至主要内容
临床试验/IRCT201212233706N19
IRCT201212233706N19已完成未知

The effect of oral Crocus Sativus (Saffron) tablet on cervical ripening in term pregnant women: a randomized controlled trial

Research deputy of Tabriz university of medical sciences0 个研究点目标入组 50 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 years 至 39 years(—)
性别
Female

入选标准

  • 1. Women with 1-3 gravidity and gestational age of 39-41 weeks 2. Not starting uterine contractions 3. Willing to deliver in Bonab hospital 4. Secondary and higher educational level 5. Bishop score of four or less 6. Singleton pregnancy 7. Cephalic presentation 8. Intact amniotic sac 9. Reactive non-stress test 10. Estimated fetal weight of 2500 to 4000 grams by ultrasound or examination.
  • Exclusion criteria: 1. History of cryotherapy or cautery of the cervix 2. History of cesarean or having any indication for cesarean section in current pregnancy 3. Diagnosed fetal anomalies 4. Cephalo-Pelvic Disproportion 5. Any known placental problem (placenta previa, placental abruption, placental insufficiency) 6. Maternal infection and systemic chronic diseases, including respiratory diseases, cardio - vascular, endocrine and... 7. Using any of the following drugs by the woman (oral hypoglycemic agents and insulin, anticoagulants such as aspirin and Warfarin ,non steroidal -anti-inflammatory drugs such as ibuprofen and naproxen, herbal drugs and antihypertensives, benzodiazepines such as lorazepam and diazepam, barbiturates such as phenobarbital, narcotics, antidepressant, Alcohol) 8. Not access to telephone line

排除标准

  • 未提供

研究者

发起方
Research deputy of Tabriz university of medical sciences

相似试验