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临床试验/IRCT2013040912958N1
IRCT2013040912958N1已完成未知

Comparison of vaginal and sub-lingual misoprestol for induction of therapeutic abortion at 12- 20 weeks gestational age 2012-13

Tehran University of Medical Sciences0 个研究点目标入组 480 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
入组人数
480

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
20 years 至 40 years(—)
性别
Female

入选标准

  • Inclusion criteria :
  • All pregnant women with gestational age between 12 and 20 weeks who have medical indications for pregnancy termination 20-40 years old including fetal indications like structural or chromosomal fetal abnormalities, PROM, intrauterine fetal death or maternal indication such as pregnant women with hemoglobin less than 10 mg.

排除标准

  • pregnant women with any type of allergic reaction to misoprestol,
  • pregnant women high risk for rupture of uterine,
  • history of classic uterine incision or T-shaped incision,
  • women with a history of extensive surgery on the fundus of the uterus, pregnant women with IUD,
  • women with certain medical conditions such as severe anemia, clotting disorders or taking anticoagulant medication, active liver disease, glaucoma, uncontrolled seizure disorders, adrenal disease or disorder that requires treatment with glucocorticoids such as tracheobronchial asthma,
  • Smoking more than 20 cigarettes per day,
  • gynecologic abnormalities confirmed by ultrasound, mitral stenosis,
  • sickle cell anemia,
  • diastolic blood pressure more than 90 mm Hg, systolic pressure less than 90 mmHg,
  • history of thromboembolism and liver disease, hemolytic disorders and a history of two cesareans.

研究者

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Misoprostol in therapeutic abortio | 临床试验